HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 413990Generated: October 29, 2026
Methyl chloroformate → methyl (S)-(1-benzyl-3-chloro-2-oxo-propyl)carbamate
https://huagongshe.com/reaction/413990
Participants
| Role | Name | HCID | Charge |
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| Reactant | Methyl chloroformate | HCID 6586 | — |
| Reactant | Sodium Bicarbonate | HCID 516892 | — |
| Reactant | (S)-3-Amino-1-chloro-4-phenylbutan-2-one hydrochloride | HCID 56777393 | — |
| Solvent | Water | HCID 962 | — |
| Solvent | Toluene | HCID 1140 | — |
| Product | methyl (S)-(1-benzyl-3-chloro-2-oxo-propyl)carbamate | HCID 9881533 | 78% |
Reaction Steps
(3S)-3-Amino-1-chloro-4-phenyl-2-butanone hydrochloride (2.0 g) was dissolved in water (34 ml). A solution (50 ml) of methyl chloroformate (0.858 ml) in toluene was added to the obtained solution. Further, an aqueous solution (15 ml) of sodium hydrogencarbonate (1.44 g) was added dropwise to the obtained mixture. They were stirred at room temperature for 1 hour to conduct the reaction. After the extraction with toluene twice and with ethyl acetate twice, the organic layers were combined together. The solvents were evaporated under reduced pressure. n-Hexane and 2-propanol were added to the residue. The obtained mixture was heated to 50° C. to obtain a homogeneous solution, which was cooled to 10° C. to form crystals. The crystals were taken by the filtration, washed with cold 2-propanol (6 ml) and then dried to obtain (3S)-3-methoxycarbonylamino-1-chloro-4-phenyl-2-butanone (1.70 g) in a yield of 78%.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US06570039B2 |
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| Source dataset | uspto-grants-2003_05 |
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| ORD ID | ord-968d060ef52d47d1948625b6ef402b3a |
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| Source note | uspto-grants-2003_05 |
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