HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2102880Generated: October 30, 2026
Dimethyl Sulfoxide → Benzyl [(1S)-3-oxo-1-phenylpropyl]carbamate
https://huagongshe.com/reaction/2102880
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Dimethyl Sulfoxide | HCID 679 | — |
| Reactant | Triethylamine | HCID 8471 | — |
| Reactant | HCID 11550966 | HCID 11550966 | — |
| Solvent | Toluene | HCID 1140 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | Benzyl [(1S)-3-oxo-1-phenylpropyl]carbamate | HCID 59710465 | — |
Reaction Steps
Sulphur trioxide pyridine complex (965 g, 6.1 mol) was slurried in dichloromethane (2 l) under an atmosphere of nitrogen. Dimethylsulfoxide (2 l) was added and the resultant solution was cooled to 0° C. A solution of benzyl (1S)-3-hydroxy-1-phenylpropylcarbamate (577 g, 2.0 mol), triethylamine (845 ml, 6.1 mol) and dimethylsulfoxide (1 l) in dichloromethane (1 ml) was added slowly to the reaction mixture keeping temperature below 10° C. The resultant yellow solution was stirred at 0° C. for 2.5 hours. A sample was analysed by TLC indicating that all starting material was consumed. Water (8.6 l) was added and a biphasic mixture was obtained. The mixture was diluted with toluene (8.6 l) and the layers were separated. The organic layer was concentrated under reduced pressure to yield a brown foam, which was taken on to Preparation 19 without further purification.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07576097B2 |
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| Source dataset | uspto-grants-2009_08 |
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| ORD ID | ord-52a7d2a8cc144b87ad592aab858e4a7d |
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| Source note | uspto-grants-2009_08 |
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