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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1770762Generated: November 3, 2026

Sodium borohydride → HCID 67515018, compound

https://huagongshe.com/reaction/1770762

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSodium borohydrideHCID 4311764—
ReactantHCID 67508114HCID 67508114—
SolventEthanolHCID 702—
ProductHCID 67515018HCID 6751501870%

Reaction Steps

Ethyl 5-(benzyloxycarbonylamino)-5-methyl-3-oxohexanoate (3.49, 10.9 mmol) was dissolved in ethanol (100 ml). Sodium borohydride (1.64 g, 43.4 mmol) was added to the mixture, and the reaction mixture was stirred for 3 hours at room temperature. The reaction was quenched with 1 N HCl, and the mixture was stirred for 1 hour. The mixture was extracted with ethylacetate, and the combined organic layers were dried over sodium sulfate, filtered, and purified by column chromatography (0 to 4% methanol on dichloromethane) to give 2.14 g (70%) of the title compound.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09248117B2
Source datasetuspto-grants-2016_02
ORD IDord-96d0914212db4294b2c2a4e23e4fd24a
Source noteuspto-grants-2016_02