Reaction #4116245
Related Literature (1)
openreactiondata ↗doi:10.1039/C8SC04228D
Conditions: temp:0.00; pressure:0.00; stir:
Source ID: ord-908e323185194dee9dc3e76c40935fb6No renderable structure data available
CCN1CCOCC1COChemical Intermediate
Structures, identifiers and computed properties have been matched to the database record by CAS.
| Intermediates | (4-ethylmorpholin-3-yl)methanol |
|---|---|
| IUPAC Name | — |
| CAS Number | 1228947-10-1 |
| Database ID | 67126464 |
| Molecular Formula | — |
| Molecular Weight | — |
Product Information
(4-ethylmorpholin-3-yl)methanol (CAS 1228947-10-1) 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 67126464
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-908e323185194dee9dc3e76c40935fb6Conditions: temp:0.00; pressure:0.00; stir:; See reaction.notes.procedure_details.
Procedure: Morpholin-3-ylmethanol (500 mg) and iodoethane (666 mg) in N,N-dimethylformamide was treated with K2CO3 (1.1 g) overnight. The reaction mixture was diluted with water and extracted with ethyl acetate. The organic layer was dried over Na2SO4 and concentrated to provide the title compound. extracted with ethyl acetate The organic layer was dried over Na2SO4 concentrated
Source ID: ord-738da105257b4ee9b6fcda23c7e4428dConditions: temp:0.00; pressure:0.00; stir:; See reaction.notes.procedure_details.
Procedure: Morpholin-3-ylmethanol (500 mg) and iodoethane (666 mg) in N,N-dimethylformamide was treated with K2CO3 (1.1 g) overnight. The reaction mixture was diluted with water and extracted with ethyl acetate. The organic layer was dried over Na2SO4 and concentrated to provide the title compound. extracted with ethyl acetate The organic layer was dried over Na2SO4 concentrated
Source ID: ord-738da105257b4ee9b6fcda23c7e4428dConditions: temp:0.00; pressure:0.00; stir:; See reaction.notes.procedure_details.
Procedure: Morpholin-3-ylmethanol (500 mg) and iodoethane (666 mg) in N,N-dimethylformamide was treated with K2CO3 (1.1 g) overnight. The reaction mixture was diluted with water and extracted with ethyl acetate. The organic layer was dried over Na2SO4, filtered, and concentrated to provide the title compound. extracted with ethyl acetate The organic layer was dried over Na2SO4 filtered concentrated
Source ID: ord-f790e436830b4a639421fc3b1f955ff8Conditions: temp:0.00; pressure:0.00; stir:; See reaction.notes.procedure_details.
Procedure: Morpholin-3-ylmethanol (500 mg) and iodoethane (666 mg) in N,N-dimethylformamide was treated with K2CO3 (1.1 g) overnight. The reaction mixture was diluted with water and extracted with ethyl acetate. The organic layer was dried over Na2SO4, filtered, and concentrated to provide the title compound. extracted with ethyl acetate The organic layer was dried over Na2SO4 filtered concentrated
Source ID: ord-f790e436830b4a639421fc3b1f955ff8Conditions: temp:0.00; pressure:0.00; stir:; See reaction.notes.procedure_details.
Procedure: Morpholin-3-ylmethanol (500 mg) and iodoethane (666 mg) in N,N-dimethylformamide was treated with K2CO3 (1.1 g) overnight. The reaction mixture was diluted with water and extracted with ethyl acetate. The organic layer was dried over Na2SO4, filtered, and concentrated to provide the title compound. extracted with ethyl acetate The organic layer was dried over Na2SO4 filtered concentrated
Source ID: ord-ad21674b06b1464fa78b2f12e5add58dConditions: temp:0.00; pressure:0.00; stir:; See reaction.notes.procedure_details.
Procedure: Morpholin-3-ylmethanol (500 mg) and iodoethane (666 mg) in N,N-dimethylformamide was treated with K2CO3 (1.1 g) overnight. The reaction mixture was diluted with water and extracted with ethyl acetate. The organic layer was dried over Na2SO4 and concentrated to provide the title compound. extracted with ethyl acetate The organic layer was dried over Na2SO4 concentrated
Source ID: ord-e2da64202d594a2080e85937fdf96ebfConditions: temp:0.00; pressure:0.00; stir:; See reaction.notes.procedure_details.
Procedure: Morpholin-3-ylmethanol (500 mg) and iodoethane (666 mg) in N,N-dimethylformamide was treated with K2CO3 (1.1 g) overnight. The reaction mixture was diluted with water and extracted with ethyl acetate. The organic layer was dried over Na2SO4 and concentrated to provide the title compound. extracted with ethyl acetate The organic layer was dried over Na2SO4 concentrated
Source ID: ord-e2da64202d594a2080e85937fdf96ebfConditions: temp:0.00; pressure:0.00; stir:; See reaction.notes.procedure_details.
Procedure: Morpholin-3-ylmethanol (500 mg) and iodoethane (666 mg) in N,N-dimethylformamide was treated with K2CO3 (1.1 g) overnight. The reaction mixture was diluted with water and extracted with ethyl acetate. The organic layer was dried over Na2SO4, filtered, and concentrated to provide the title compound. extracted with ethyl acetate The organic layer was dried over Na2SO4 filtered concentrated
Source ID: ord-89f4f5fb74a748d9b48714a2051899e8Conditions: temp:0.00; pressure:0.00; stir:; See reaction.notes.procedure_details.
Procedure: Morpholin-3-ylmethanol (500 mg) and iodoethane (666 mg) in N,N-dimethylformamide was treated with K2CO3 (1.1 g) overnight. The reaction mixture was diluted with water and extracted with ethyl acetate. The organic layer was dried over Na2SO4 and concentrated to provide the title compound. extracted with ethyl acetate The organic layer was dried over Na2SO4 concentrated
Source ID: ord-65c65c693aa74d53bc9f33f6483e069aConditions: temp:0.00; pressure:0.00; stir:; See reaction.notes.procedure_details.
Procedure: Morpholin-3-ylmethanol (500 mg) and iodoethane (666 mg) in N,N-dimethylformamide was treated with K2CO3 (1.1 g) overnight. The reaction mixture was diluted with water and extracted with ethyl acetate. The organic layer was dried over Na2SO4 and concentrated to provide the title compound. extracted with ethyl acetate The organic layer was dried over Na2SO4 concentrated
Source ID: ord-65c65c693aa74d53bc9f33f6483e069aConditions: temp:0.00; pressure:0.00; stir:
Source ID: ord-908e323185194dee9dc3e76c40935fb6PubChem References
These sources are listed in the compound's public database record.
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