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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1734284Generated: November 1, 2026

Sodium Hydroxide → HCID 22399683, compound

https://huagongshe.com/reaction/1734284

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSodium HydroxideHCID 14798—
ReactantAmmonium AcetateHCID 517165—
ReactantSodium cyanoborohydrideHCID 5003444—
ReactantHCID 67766280HCID 67766280—
SolventMethanolHCID 887—
ProductHCID 22399683HCID 22399683—

Reaction Steps

A mixture of benzyltrimethylsilylketone (1.40 g, 7.3 mmol) of sodium cyanoborohydride (0.321 g, 5.1 mmol) and ammonium acetate (5.93 g, 73 mmol) in anhydrous methanol (25 ml) was stirred at room temperature for 48 hours. The mixture was poured into 2N sodium hydroxide (20 ml) and extracted with diethyl ether (3×100 ml). The organic phase was dried over anhydrous magnesium sulphate. Trituration, removal of the solvent, inuacuo, and chromatography from silica gel (ethyl acetate/cyclohexane 1:1) yielded the crude α-(trimethylsilyl)benzeneethanamine which was directly converted to the product of this step using 1 equivalent of (BOC)2O in THF. Rf: 0.74 (ethyl acetate/cyclohexane 1:1)

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05532397
Source datasetuspto-grants-1996_07
ORD IDord-74f5f2e923044441bba1b0cd2b453e05
Source noteuspto-grants-1996_07