Reaction #4163775
Related Literature (1)
openreactiondata ↗doi:10.1039/C8SC04228D
Conditions: temp:0.00; pressure:0.00; stir:
Source ID: ord-c68ab11fbd884c0191712787a0f1212cNo renderable structure data available
C1CCC(CC1)N2CCCC2=OChemical Intermediate
Structures, identifiers and computed properties have been matched to the database record by CAS.
| Intermediates | 1-cyclohexylpyrrolidin-2-one |
|---|---|
| IUPAC Name | — |
| CAS Number | 6837-24-7 |
| Database ID | 81278 |
| Molecular Formula | — |
| Molecular Weight | — |
Product Information
1-cyclohexylpyrrolidin-2-one (CAS 6837-24-7) product identity, structure identifiers and related reaction data for chemical intermediate research and sourcing review.
Potential Applications
For professional research and industrial use only
Database ID 81278
Safety Notice
For professional research and industrial use only. Review the supplier safety data sheet before handling.
Synthesis data
12 reactions · 12 references
Conditions: temp:0.00; pressure:0.00; stir:
Source ID: ord-c68ab11fbd884c0191712787a0f1212cConditions: temp:0.00; pressure:0.00; stir:
Source ID: ord-c43c7f173fe64fa0b668295b4cf11f96Conditions: temp:0.00; pressure:0.00; stir:
Source ID: ord-29749cf6fb4b4d5495829c5240950533Conditions: temp:-78.01; pressure:0.00; stir:; See reaction.notes.procedure_details.
Procedure: Dissolve commercially available 1-cyclohexyl-pyrrolidin-2-one (88.2 g, 527.9 mmol) in 2500 mL tetrahydrofuran and cool to −78° C. Add 176 mL 2 M LDA and stir for ˜5 min. Add 2-bromomethyl-1,3-dichloro-5-methoxy-benzene (95 g, 351.9 mmol) and allow the reaction to warm to room temperature. Pour the mixture into saturated ammonium chloride and extract twice with dichloromethane. Dry over sodium sulfate, filter and concentrate under vacuum to obtain a tan solid. Add hexanes and stir rapidly before filtering. Wash the filter cake several times with cold hexane to obtain 86 g (69%) of a light-tan solid: MS (m/z): 356 (M+). the reaction to warm to room temperature extract twice with dichloromethane Dry over sodium sulfate filter concentrate under vacuum to obtain a tan solid before filtering Wash the filter cake several times with cold hexane
Source ID: ord-671ed090c526489ea143d527e9a47bc2Conditions: temp:0.00; pressure:0.00; stir:
Source ID: ord-c68ab11fbd884c0191712787a0f1212cConditions: temp:0.00; pressure:0.00; stir:
Source ID: ord-c43c7f173fe64fa0b668295b4cf11f96Conditions: temp:0.00; pressure:0.00; stir:
Source ID: ord-c43c7f173fe64fa0b668295b4cf11f96Conditions: temp:0.00; pressure:0.00; stir:; See reaction.notes.procedure_details.
Procedure: An ink composition comprising 2.5 percent by weight of Tartrazine FD&C Yellow #5, a yellow dye obtained from Buffalo Color, West Patterson, N.Y., 15 percent by weight of cyclohexyl pyrrolidone (obtained from GAF Corporation, Wayne, N.J.), and 82.5 percent by weight of deionized water was prepared by mixing together the ingredients at room temperature, stirring to obtain a homogeneous solution, and filtering. An additional ink was also prepared, said ink being of the same composition as the first except that it contained 0.3 percent by weight of Carbowax M20. The Carbowax M20 was added to the ink at room temperature and the resulting mixture was stirred for about 5 minutes to obtain a homogeneous solution. by mixing together the ingredients at room temperature to obtain a homogeneous solution filtering An additional ink was also prepared the resulting mixture was stirred for about 5 minutes to obtain a homogeneous solution
Source ID: ord-74e116988dff4692a79491e5ca5c919cConditions: temp:0.00; pressure:0.00; stir:; See reaction.notes.procedure_details.
Procedure: An ink composition comprising 2.5 percent by weight of Tartrazine FD&C Yellow #5, a yellow dye obtained from Buffalo Color, West Patterson, N.Y., 15 percent by weight of cyclohexyl pyrrolidone (obtained from GAF Corporation, Wayne, N.J.), and 82.5 percent by weight of deionized water was prepared by mixing together the ingredients at room temperature, stirring to obtain a homogeneous solution, and filtering. An additional ink was also prepared, said ink being of the same composition as the first except that it contained 0.3 percent by weight of Carbowax M20. The Carbowax M20 was added to the ink at room temperature and the resulting mixture was stirred for about 5 minutes to obtain a homogeneous solution. by mixing together the ingredients at room temperature to obtain a homogeneous solution filtering An additional ink was also prepared the resulting mixture was stirred for about 5 minutes to obtain a homogeneous solution
Source ID: ord-74e116988dff4692a79491e5ca5c919cConditions: temp:-78.01; pressure:0.00; stir:; See reaction.notes.procedure_details.
Procedure: Dissolve commercially available 1-cyclohexyl-pyrrolidin-2-one (88.2 g, 527.9 mmol) in 2500 mL tetrahydrofuran and cool to −78° C. Add 176 mL 2 M LDA and stir for ˜5 min. Add 2-bromomethyl-1,3-dichloro-5-methoxy-benzene (95 g, 351.9 mmol) and allow the reaction to warm to room temperature. Pour the mixture into saturated ammonium chloride and extract twice with dichloromethane. Dry over sodium sulfate, filter and concentrate under vacuum to obtain a tan solid. Add hexanes and stir rapidly before filtering. Wash the filter cake several times with cold hexane to obtain 86 g (69%) of a light-tan solid: MS (m/z): 356 (M+). the reaction to warm to room temperature extract twice with dichloromethane Dry over sodium sulfate filter concentrate under vacuum to obtain a tan solid before filtering Wash the filter cake several times with cold hexane
Source ID: ord-671ed090c526489ea143d527e9a47bc2Conditions: temp:0.00; pressure:0.00; stir:; See reaction.notes.procedure_details.
Procedure: An ink composition comprising 2.5 percent by weight of Tartrazine FD&C Yellow #5, a yellow dye obtained from Buffalo Color, West Patterson, N.Y., 15 percent by weight of cyclohexyl pyrrolidone (obtained from GAF Corporation, Wayne, N.J.), and 82.5 percent by weight of deionized water was prepared by mixing together the ingredients at room temperature, stirring to obtain a homogeneous solution, and filtering. An additional ink was also prepared, said ink being of the same composition as the first except that it contained 0.3 percent by weight of Carbowax M20. The Carbowax M20 was added to the ink at room temperature and the resulting mixture was stirred for about 5 minutes to obtain a homogeneous solution. by mixing together the ingredients at room temperature to obtain a homogeneous solution filtering An additional ink was also prepared the resulting mixture was stirred for about 5 minutes to obtain a homogeneous solution
Source ID: ord-74e116988dff4692a79491e5ca5c919cConditions: temp:0.00; pressure:0.00; stir:; See reaction.notes.procedure_details.
Procedure: An ink composition comprising 2.5 percent by weight of Tartrazine FD&C Yellow #5, a yellow dye obtained from Buffalo Color, West Patterson, N.Y., 15 percent by weight of cyclohexyl pyrrolidone (obtained from GAF Corporation, Wayne, N.J.), and 82.5 percent by weight of deionized water was prepared by mixing together the ingredients at room temperature, stirring to obtain a homogeneous solution, and filtering. An additional ink was also prepared, said ink being of the same composition as the first except that it contained 0.3 percent by weight of Carbowax M20. The Carbowax M20 was added to the ink at room temperature and the resulting mixture was stirred for about 5 minutes to obtain a homogeneous solution. by mixing together the ingredients at room temperature to obtain a homogeneous solution filtering An additional ink was also prepared the resulting mixture was stirred for about 5 minutes to obtain a homogeneous solution
Source ID: ord-be3efbcf3dc141dc81dfa55a22b25b70PubChem References
These sources are listed in the compound's public database record.
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