HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1532833Generated: October 30, 2026
Sodium borohydride → [4-Hydroxymethyl-2-phenylbenzoyl]methionine methyl ester
https://huagongshe.com/reaction/1532833
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Sodium borohydride | HCID 4311764 | — |
| Reactant | 4-Formyl-2-phenylbenzoyl methionine methyl ester | HCID 10571267 | — |
| Solvent | Ethanol | HCID 702 | — |
| Product | [4-Hydroxymethyl-2-phenylbenzoyl]methionine methyl ester | HCID 20622833 | — |
Reaction Steps
To a solution of the resultant compound from Example 16E in ethanol at 0° C. is added sodium borohydride (0.5 equivalent), and the reaction is stirred at 0° C. until TLC analysis shows the reaction to be complete. The reaction mixture is extracted with ether, which is washed with water and brine, dried over anhydrous magnesium sulfate, filtered, and concentrated in vacuo. The residue is then purified by column chromatography on silica gel to afford the title product.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US06204293B1 |
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| Source dataset | uspto-grants-2001_03 |
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| ORD ID | ord-6d13e76796164a49a32290d07cf7cdf2 |
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| Source note | uspto-grants-2001_03 |
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