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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1956623Generated: November 3, 2026

Thiophosgene → N-(2-tert-butyldimethysilyloxy-4-nitrophenyl)-N'-phenyl-thiourea

https://huagongshe.com/reaction/1956623

Reaction equation

Participants

RoleNameHCIDCharge
ReactantThiophosgeneHCID 10040—
ReactantSodium BicarbonateHCID 516892—
Reactant2-[(Tert-butyldimethylsilyl)oxy]-4-nitroanilineHCID 15485710—
SolventChloroform waterHCID 22418719—
ProductN-(2-tert-butyldimethysilyloxy-4-nitrophenyl)-N'-phenyl-thioureaHCID 1552427898%

Reaction Conditions

Temperature23 °C

Reaction Steps

N-(2-tert-Butyldimethysilyloxy-4-nitrophenyl)-N'-phenyl-thiourea was prepared by treating a biphasic solution of 2-tert-butyldimethysilyloxy-4-nitroaniline(80 mg, 0.308 mmol) and NaHCO3 in CHCl3 :H2O(2.5:1, 7 mL) with thiophosgene at 0° C. The solution was allowed to warm to 23° C. and the reaction was continued overnight. The CHCl3 layer was separated and dried over sodium sulfate. The solution was concentrated in vacuo and the residue was dissolved in toluene and treated with aniline (100 uL) at 23° C. for 12 h. The reaction mixture was concentrated and the residue was purified by flash chromatography (10% EtOAc/hexanes) to afford the titled compound as a yellow solid (120.8 mg, 98%) mp: 144°-145° C.;1H NMR (CD3OD/CDCl3): d 8.65 (d, 1H, J=10.0 Hz), 7.58 (d, 1H, J=10.0 Hz), 7.47 (d, 1H, J=1.25 Hz), 7.26 (m, 4H), 7.10(m, 1H).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05780483
Source datasetuspto-grants-1998_07
ORD IDord-69d5c96903d6488b97fc9b1004f9655c
Source noteuspto-grants-1998_07