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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2418770Generated: November 2, 2026

Sodium borohydride → HCID 54529640, compound

https://huagongshe.com/reaction/2418770

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSodium borohydrideHCID 4311764—
ReactantHCID 53803015HCID 53803015—
SolventEthanolHCID 702—
ProductHCID 54529640HCID 54529640—

Reaction Steps

A solution of 3-(S)-t-butyloxycarbonylamino-1-ethoxycarbonylmethyl-2,3,4,5,5a,6,7,8,9,9a-decahydro-1H-[1]benzazepin-2,5-dione (2.7 g) and sodium borohydride (0.2 g) in ethanol (100 ml) is stirred at room temperature for 18 hours. The solvent is removed under reduced pressure, and the residue dissolved in dichloromethane (100 ml). The solution is extracted with ice-cold 2N HCl (2×50 ml) and saturated brine (50 ml) and dried over sodium sulfate. The solvent is removed under reduced pressure and the residue triturated with ether to give 3-(S)-t-butyloxycarbonylamino-1-ethoxycarbonylmethyl-5-hydroxy-2,3,4,5,5a,6,7,8,9,9a-decahydro-1H-[1]benzazepin-2-one.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04473575
Source datasetuspto-grants-1984_09
ORD IDord-5f62ae2959644d06b8ae4cfd6fa5b81c
Source noteuspto-grants-1984_09