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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1085674Generated: November 1, 2026

2-Aminophenol → HCID 20060589, compound

https://huagongshe.com/reaction/1085674

Reaction equation

Participants

RoleNameHCIDCharge
Reactant2-AminophenolHCID 5801—
ReactantSulfurHCID 5362487—
ReactantEthyl 3-isothiocyanatopyrrolidine-1-carboxylateHCID 14575268—
CatalystMercuric oxideHCID 30856—
SolventAcetonitrileHCID 6342—
ProductHCID 20060589HCID 2006058964%

Reaction Steps

A mixture of 55 parts of ethyl 3-isothiocyanato-1-pyrrolidinecarboxylate, 23.6 parts of 2-aminophenol and 320 parts of acetonitrile was stirred and refluxed for 4 hours. Then there were added 93 parts of mercury(II) oxide and 0.5 parts of sulfur while stirring vigorously. The reaction mixture was stirred and refluxed overnight. After cooling, the mixture was filtered over diatomaceous earth and the filtrate was evaporated. The residue was purified by column chromatography over silica gel using a mixture of trichloromethane and methanol (99:1 by volume) as eluent. The pure fractions were collected and the eluent was evaporated, yielding 38 parts (64%) of ethyl 3-[(2-benzoxazolyl)amino]-1-pyrrolidinecarboxylate as a residue (38).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05010198
Source datasetuspto-grants-1991_04
ORD IDord-241ca1f2631447fe834d777bc88ff799
Source noteuspto-grants-1991_04