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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 53573Generated: October 27, 2026

Carbon Dioxide → 2-Hydroxybenzenecarbothioamide

https://huagongshe.com/reaction/53573

Reaction equation

Participants

RoleNameHCIDCharge
ReactantCarbon DioxideHCID 280—
ReactantSodium ChlorideHCID 5234—
ReactantO,O-Diethyl dithiophosphateHCID 9274—
Reactant2-HydroxybenzonitrileHCID 11907—
ReactantSodium BicarbonateHCID 516892—
SolventWaterHCID 962—
SolventDiethyl EtherHCID 3283—
SolventDichloromethaneHCID 6344—
Product2-HydroxybenzenecarbothioamideHCID 275934255%

Reaction Steps

A stirred solution of 2-hydroxybenzonitrile (23.8 g, 200 mmol), (EtO)2P(S)SH (33.6 mL, 200 mmol) and water (40 mL) was heated at 80° C. for 12 hr under nitrogen. The mixture was cooled down to 0°-10° C., diluted with CH2Cl2 (200 mL)/Et2O (400 mL), then cautiously treated with saturated aq. NaHCO3 (60 mL), and followed by adding solid NaHCO3 in small portions until CO2 evolution ceased. Half-saturated aq. NaCl (40 mL) was added to the mixture. The organic layer was separated, washed with brine (100 mL), dried over MgSO4, and filtered. After concentration in vacuo, the residue was chromatographed on silica gel (gradient EtOAc/CH2Cl2 :0-5%) to give 3a (16.7 g, 55%) as a pinkish solid, which had the same 1HNMR data as reported in the literature (Yousif, N. M. Tetrahedron 1989, 45, 4599).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05620968
Source datasetuspto-grants-1997_04
ORD IDord-a726745185ea4e27ab755f57b036fc7d
Source noteuspto-grants-1997_04