Reaction #4133318
Related Literature (1)
openreactiondata ↗doi:10.1039/C8SC04228D
Conditions: temp:0.00; pressure:0.00; stir:
Source ID: ord-a1ace13d61e043af9ca45b794bcbe08bNo renderable structure data available
C(COCCCl)OChemical Intermediate
Structures, identifiers and computed properties have been matched to the database record by CAS.
| Intermediates | 2-(2-chloroethoxy)ethanol |
|---|---|
| IUPAC Name | — |
| CAS Number | 52137-03-8 |
| Database ID | 12361 |
| Molecular Formula | — |
| Molecular Weight | — |
Product Information
2-(2-chloroethoxy)ethanol (CAS 52137-03-8) 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 12361
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-a1ace13d61e043af9ca45b794bcbe08bConditions: temp:0.00; pressure:0.00; stir:
Source ID: ord-440f202a51a44a58a546f07ac91ae8a6Conditions: temp:0.00; pressure:0.00; stir:
Source ID: ord-d4d3be5f44cc46fab83a05a4cb44513cConditions: temp:0.00; pressure:0.00; stir:
Source ID: ord-53e3c98e21044b9a8a4343037c7ac5ecConditions: temp:0.00; pressure:0.00; stir:
Source ID: ord-631bbb60532448e9a0b9b9d8762247aaConditions: temp:0.00; pressure:0.00; stir:
Source ID: ord-bd31cf4bda134528830db16e9b7247b9Conditions: temp:0.00; pressure:0.00; stir:
Source ID: ord-a4a1e96bc3a046d2b6cc56a5566a3b6dConditions: temp:0.00; pressure:0.00; stir:
Source ID: ord-849c38469205436b95496e375f8ff2d0Conditions: temp:0.00; pressure:0.00; stir:
Source ID: ord-d81b069b0c5d472cae4d9e612d268a90Conditions: temp:0.00; pressure:0.00; stir:
Source ID: ord-f37b97c236e54382bb6f9e2ca2bdeae1Conditions: temp:70.01; pressure:0.00; stir:; See reaction.notes.procedure_details.
Procedure: To a solution of 2-(2-chloroethoxy)ethanol 14 (5 mL, 47.4 mmol) in N,N-dimethylformamide (35 mL) was added potassium phthalimide 2 (8.8 g, 47.51 mmol), and the reaction mixture was stirred for 20 h at 70° C. The mixture was concentrated and then diluted with dichloromethane (300 mL), and the organic layer was washed with water, dried, and concentrated. The residue was purified by flash column chromatography (3:2 to 2:3 hexane-ethyl acetate) to give compound 15 as a white solid (7.15 g, 64.17%) having an RF of 0.12 (solvent 3:2 hexane-ethyl acetate). See FIG. 9. The mixture was concentrated diluted with dichloromethane (300 mL) the organic layer was washed with water dried concentrated The residue was purified by flash column chromatography (3:2 to 2:3 hexane-ethyl acetate)
Source ID: ord-cf405ceb7bdf43ffb257a0be49cbc372Conditions: temp:85.01; pressure:0.00; stir:; See reaction.notes.procedure_details.
Procedure: A mixture of 400 mg (0.746 mmol) N-(3,5-bis-trifluoromethyl-benzyl)-N-methyl-6-piperazin-1-yl-4-o-tolyl-nicotinamide (Example 53), 0.18 ml (1.7 mmol) 2-(2-chloroethoxy)-ethanol and 0.189 g (1.35 mmol) potassium carbonate in 8 ml acetonitrile was stirred at 85° C. for 48 h. After cooling to room temperature 40 ml 1 N sodium hydroxide solution were added. Extraction with 3 60-ml portions of dichloromethane, drying with sodium sulfate and concentration gave 528 mg of the crude product. Flash column chromatography afforded 300 mg (64.4%) of the title compound as a light-brown solid. were added Extraction with 3 60-ml portions of dichloromethane drying with sodium sulfate and concentration gave 528 mg of the crude product
Source ID: ord-f700a9ab02e34db28dc82b73bf8a7668PubChem References
These sources are listed in the compound's public database record.
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