HuagongsheHuagongshe Chemistry Print Report · For research reference only
Sodium borohydride → 2-(2-Biphenyl-4-yl-furan-5-yl)-2-hydroxy-acetic acid ethyl ester
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Sodium borohydride | HCID 4311764 | — |
| Reactant | 1-(4(S)-benzyl-2, 2-dimethyl-oxazolidin-3-yl)-2-(biphenyl-4-yl-1H-pyrrol-3-yl)-2-hydroxy-ethanone | HCID 18341257 | — |
| Reactant | 2-(2-Biphenyl-4-yl-furan-5-yl)-2-oxoacetic acid ethyl ester | HCID 18341512 | — |
| Product | 2-(2-Biphenyl-4-yl-furan-5-yl)-2-hydroxy-acetic acid ethyl ester | HCID 18341511 | — |
Reaction Steps
According to the procedure described in Example 13 for the preparation of 1-(4(S)-benzyl-2,2-dimethyl-oxazolidin-3-yl)-2-(biphenyl-4-yl-1H-pyrrol-3-yl)-2-hydroxy-ethanone, 2-(2-biphenyl-4-yl-furan-5-yl)-2-oxoacetic acid ethyl ester was reduced with NaBH4 to give in quantitative yield 2-(2-biphenyl-4-yl-furan-5-yl)-2-hydroxy-acetic acid ethyl ester as a yellow solid, mp 75-80° C. (d), which was used crude without purification.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US06306892B1 |
| Source dataset | uspto-grants-2001_10 |
| ORD ID | ord-48ddb6691f8549bfbbade74094633c04 |
| Source note | uspto-grants-2001_10 |