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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2296969Generated: October 30, 2026

Ammonium Chloride → 3-(1-(Benzyloxyimino)ethyl)benzylalcohol

https://huagongshe.com/reaction/2296969

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAmmonium ChlorideHCID 25517—
ReactantSodium borohydrideHCID 4311764—
Reactant3-(1-(Benzyloxyimino)ethyl)benzaldehydeHCID 73433317—
SolventMethanolHCID 887—
SolventTetrahydrofuranHCID 8028—
Product3-(1-(Benzyloxyimino)ethyl)benzylalcoholHCID 8675863096.5%

Reaction Steps

To a solution of 9.92 g (39.17 mmol) of 3-(1-(benzyloxyimino)ethyl)benzaldehyde in 70 ml of dry methanol and 70 ml of dry tetrahydrofuran was added 1.81 g (43 mmol) of sodium borohydride portionwise with ice-cooling, and the mixture was stirred for 2 hours with ice-cooling. Further, 0.30 g of sodium borohydride portionwise was added thereto with ice-cooling, and the mixture was stirred for 2 hours with ice-cooling. The reaction mixture was poured into 500 ml of an about 5% aqueous solution of ammonium chloride, and the mixture was extracted with tert-butyl methyl ether. The organic layer was dried and concentrated to obtain 9.64 g (37.8 mmol) of 3-(1-(benzyloxyimino)ethyl)benzylalcohol.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06489487B1
Source datasetuspto-grants-2002_12
ORD IDord-565bdc0af0c14cd8850cc433c1c28e52
Source noteuspto-grants-2002_12