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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1722518Generated: November 2, 2026

Hydrochloric Acid → Methyl 2-(2-chlorobenzylaminooxymethyl)-2-methylpropanoate

https://huagongshe.com/reaction/1722518

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydrochloric AcidHCID 313—
ReactantMethyl 2-(2-chlorobenzylideneaminooxymethyl)-2-methylpropanoateHCID 54572932—
SolventEthanolHCID 702—
ProductMethyl 2-(2-chlorobenzylaminooxymethyl)-2-methylpropanoateHCID 2002922828.5%

Reaction Steps

A mixture of methyl 2-(2-chlorobenzylideneaminooxymethyl)-2-methylpropanoate (10.0 grams, 0.04 mole) and borane-pyridine complex (10.4 mL; 0.12 mole) in absolute ethanol (30 mL) was cooled in an ice bath. A solution of anhydrous 6.5N hydrogen chloride in ethanol (60 mL) was then added slowly. Upon completion of addition, the reaction mixture was stirred at ambient temperature for four hours. The reaction mixture was concentrated under reduced pressure, and methylene chloride (50 mL) was added to the residue. Aqueous sodium carbonate was then added to adjust the pH to 6-7. The layers were separated, and the organic layer was dried (magnesium sulfate) and concentrated under reduced pressure to yield a mixture of a white solid and liquid. The liquid was decanted off and purified by chromatography through silica gel, eluting successively with hexane and 20:1 hexane:ethyl acetate. Appropriate fractions were combined and concentrated at reduced pressure to yield 3.1 grams of methyl 2-(2-chlorobenzylaminooxymethyl)-2-methylpropanoate as a colorless liquid.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04855480
Source datasetuspto-grants-1989_08
ORD IDord-c20c420274864f7495627179251c996a
Source noteuspto-grants-1989_08