Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 376792Generated: October 30, 2026

Hydrochloric Acid → HCID 19359164, compound

https://huagongshe.com/reaction/376792

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydrochloric AcidHCID 313—
ReactantTriethylamineHCID 8471—
Reactant2-(tert-Butoxycarbonyloxyimino)-2-phenylacetonitrileHCID 93865—
ReactantHCID 19044177HCID 19044177—
SolventWaterHCID 962—
SolventTetrahydrofuranHCID 8028—
ProductHCID 19359164HCID 1935916487%

Reaction Conditions

Temperature0 °C

Reaction Steps

A suspension of 4-chloro-3-aminomethylbenzoic acid.circle-solid.HCl (6.7 g, 30 mmol) and triethylamine (9.3 g, 92 mmol) in 50 ml of H2O, was added to a solution of Boc-ON (9.2 g, 38 mmol) in 50 ml of tetrahydrofuran cooled to 0° C. The reaction mixture was stirred at room temperature overnight, and the volatile compounds were removed by concentration under reduced pressure. The residue was diluted with H2O, washed with ether, acidified to pH 3 with 1N HCl, and extracted with ethyl acetate. The extracts were washed with H2O, brine, dried over anhydrous magnesium sulfate, and evaporated to dryness under reduced pressure. This material was triturated with ether-hexane to provide the title compound (7.4 g, 87%) as a white powder. mp 159° C. (dec);

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06022523
Source datasetuspto-grants-2000_02
ORD IDord-02820cd03e0d4c90a0986262f401e3fe
Source noteuspto-grants-2000_02