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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1417895Generated: October 31, 2026

Hydrochloric Acid → HCID 19359181, compound

https://huagongshe.com/reaction/1417895

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydrochloric AcidHCID 313—
ReactantTriethylamineHCID 8471—
Reactant2-(tert-Butoxycarbonyloxyimino)-2-phenylacetonitrileHCID 93865—
ReactantHCID 17791945HCID 17791945—
SolventWaterHCID 962—
SolventTetrahydrofuranHCID 8028—
ProductHCID 19359181HCID 1935918159%

Reaction Conditions

Temperature0 °C

Reaction Steps

A suspension of 3-aminomethyl-6-iodobenzoic acid.HCl (8.0 g, 26 mmol) and triethylamine (8.7 g, 86 mmol) in 32 ml of H2O, was added to a solution of Boc-ON (8.0 g, 32 mmol) in 23 ml of tetrahydrofuran cooled to 0° C. The reaction mixture was stirred at room temperature for 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 from ether to provide the title compound (5.7 g, 59%) as a white powder; mp 182° C. (dec); 1H NMR (D6-DMSO) 13.35 (br s, 1H), 7.95 (d, 1H), 7.60 (s, 1H), 7.50 (br t, 1H), 7.10 (d, 1H), 4.10 (d, 2H), 1.40 (s, 9H).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05879657
Source datasetuspto-grants-1999_03
ORD IDord-f6eebc91603e4f78a4889ab4d94fe4d3
Source noteuspto-grants-1999_03