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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1780284Generated: November 1, 2026

Hydrochloric Acid → HCID 19049900, compound

https://huagongshe.com/reaction/1780284

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydrochloric AcidHCID 313—
ReactantEthyl bromoacetateHCID 7748—
ReactantSodium hydrideHCID 24758—
ReactantBenzyl (4-hydroxyphenyl)carbamateHCID 293061—
SolventDimethylformamideHCID 6228—
ProductHCID 19049900HCID 1904990086.4%

Reaction Steps

1.89 g (45.2 mmol) of sodium hydride (as a 55% w/w dispersion in mineral oil) were added, whilst ice-cooling, to a solution of 10.0 g (41.1 mmol) of 4-(benzyloxycarbonylamino)phenol [prepared as described in step (a) above] in 100 ml of dimethylformamide, and the mixture was stirred for 5 minutes. 5.01 ml (45.2 mmol) of ethyl bromoacetate were then added to the resulting mixture, after which the mixture was stirred at room temperature for 3 hours. At the end of this time, the reaction mixture was neutralized with 1N aqueous hydrochloric acid, and the solvent was removed by distillation under reduced pressure. The residue was mixed with ethyl acetate, and the resulting organic solution was washed with a 5% w/v aqueous solution of citric acid, with a 5% w/v aqueous solution of sodium hydrogencarbonate and with a saturated aqueous solution of sodium chloride, in that order. The reaction mixture was then dried over anhydrous sodium sulfate, and the organic solvent was removed by distillation under reduced pressure. The residue was purified by column chromatography through silica gel, using a gradient elution method, with mixtures of hexane and ethyl acetate in ratios ranging from 10:1 to 6:1 by volume as the eluent, to give 11.7 g of the title compound as colorless crystals, melting at 85°-86° C.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05629406
Source datasetuspto-grants-1997_05
ORD IDord-5b6e8114ca4543c9a875c9efff3f120f
Source noteuspto-grants-1997_05