HuagongsheHuagongshe Chemistry Print Report · For research reference only
Water → methyl N-[(4-bromophenyl)sulfonyl]-L-valinate
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Water | HCID 962 | — |
| Reactant | p-Bromobenzenesulfonyl chloride | HCID 7396 | — |
| Reactant | Sodium Carbonate | HCID 10340 | — |
| Reactant | Methyl valinate hydrochloride | HCID 111190 | — |
| Solvent | Acetone | HCID 180 | — |
| Product | methyl N-[(4-bromophenyl)sulfonyl]-L-valinate | HCID 47337186 | 84.5% |
Reaction Steps
To a suspension of methyl valinate hydrochloride (10.0 g, 59.7 mmol) and sodium carbonate (15.8 g, 149 mmol) in acetone (200 ml)-water (100 mL) was added 4-bromobenzenesulfonyl chloride (12.7 g, 49.7 mmol) at 0° C., and the mixture was stirred at room temperature for 12 hr after addition. The reaction mixture was concentrated under reduced pressure, and the residue was diluted with ethyl acetate, washed with 0.1N hydrochloric acid, water and saturated brine, and dried over sodium sulfate. The solvent was evaporated under reduced pressure, and the residue was crystallized from hexane-ethyl acetate to give the title compound as a white powder (14.7 g, 84%).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US07915267B2 |
| Source dataset | uspto-grants-2011_03 |
| ORD ID | ord-18a2087bacef4f858c652956d4472523 |
| Source note | uspto-grants-2011_03 |