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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1746046Generated: October 31, 2026

Thiophosgene → HCID 90415948, compound

https://huagongshe.com/reaction/1746046

Reaction equation

Participants

RoleNameHCIDCharge
ReactantThiophosgeneHCID 10040—
ReactantSodium HydroxideHCID 14798—
Reactant3,5-Difluoro-1,2-benzenediolHCID 21707933—
SolventChloroformHCID 6212—
ProductHCID 90415948HCID 9041594882%

Reaction Conditions

Temperature7.5 °C

Reaction Steps

3,5-Difluorobenzene-1,2-diol (670 mg, 4.6 mmol) was stirred in dry chloroform (8 mL), treated with thiophosgene (580 mg, 5.0 mmol), cooled to 5-10° C., and treated dropwise with 10% NaOH solution (4.2 g, 11 mmol) over 45 min. After 30 min, the volatiles were removed by rotary evaporation and the residual solid was collected by filtration and washed with water. The solid was dissolved in ethyl acetate (30 mL), washed with water (2×20 mL), washed with saturated NaCl (1×10 mL), dried (Na2SO4), and evaporated. The residue was purified by chromatography on silica with a 0-20% ethyl acetate-hexane gradient to give the title compound (710 mg, 82%): 1H NMR (400 MHz, CDCl3) δ 6.95 (ddd, J=6.8, 2.3, 1.4 Hz, 1H), 6.89 (td, J=9.5, 2.3 Hz, 1H); 19F NMR (376 MHz, CDCl3) δ −109.99 (s), −127.93 (s); EIMS m/z 188.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09149038B2
Source datasetuspto-grants-2015_10
ORD IDord-58e9fbce5d0640a88daeba31d5d7ee8e
Source noteuspto-grants-2015_10