HuagongsheHuagongshe Chemistry Print Report · For research reference only
HCID 2756026, compound → tert-butyl (1S)-1-benzyl-2-hydroxypropylcarbamate
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | HCID 2756026 | HCID 2756026 | — |
| Reactant | Sodium borohydride | HCID 4311764 | — |
| Solvent | Ethanol | HCID 702 | — |
| Product | tert-butyl (1S)-1-benzyl-2-hydroxypropylcarbamate | HCID 14212468 | 100.7% |
Reaction Steps
The process is performed as in Example 3, starting with 2.66 g of tert-butyl (1S)-1-benzyl-2-oxopropylcarbamate in 25 cm3 of ethanol, with 0.58 g of sodium borohydride. After 4 h 30 min at a temperature in the region of 20° C., the reaction mixture is worked up in an identical manner. 2.7 g of tert-butyl (1S)-1-benzyl-2-hydroxypropylcarbamate are obtained in the form of a white solid melting at 125° C., as a mixture of the two diastereoisomers (70/30).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US06699895B2 |
| Source dataset | uspto-grants-2004_03 |
| ORD ID | ord-a16f5264168242eeb42d9d57d61e37da |
| Source note | uspto-grants-2004_03 |