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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 966963Generated: October 26, 2026

Triphenylphosphine → [(3R)-3-[(2,5-Dichlorophenyl)thio]-3-(2-thiazolyl)propyl]carbamic acid 1,1-dimethylethyl ester

https://huagongshe.com/reaction/966963

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTriphenylphosphineHCID 11776—
ReactantDiisopropyl diazene-1,2-dicarboxylateHCID 75555—
Reactant2,5-DichlorobenzenethiolHCID 79965—
Reactant[(3S)-3-Hydroxy-3-(2-thiazolyl)propyl]carbamic acid 1,1-dimethylethyl esterHCID 69799613—
Solvent2-MethylpentaneHCID 7892—
SolventTetrahydrofuranHCID 8028—
SolventEthyl AcetateHCID 8857—
Product[(3R)-3-[(2,5-Dichlorophenyl)thio]-3-(2-thiazolyl)propyl]carbamic acid 1,1-dimethylethyl esterHCID 8675985621%

Reaction Steps

To a solution of 2,5-dichlorothiophenol (179 mg, 1 mmol), [(3S)-3-hydroxy-3-(2-thiazolyl)propyl]carbamic acid 1,1-dimethylethyl ester (258 mg, 1 mmol) and triphenylphosphine (315 mg, 1.2 mmol) in dry tetrahydrofuran (30 ml) at 0° C. under nitrogen, was added diisopropyl azodicarboxylate (243 mg, 0.24 ml, 1.2 mmol) dropwise over 5 minutes. The mixture was stirred at room temperature for 16 h, then concentrated in vacuo to leave a crude yellow gum. Flash chromatography (silica, 15% ethyl acetate in isohexane) afforded a clear oil (85 mg, 21%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06953797B2
Source datasetuspto-grants-2005_10
ORD IDord-b7d71d8b2993495cb1602eda97538b96
Source noteuspto-grants-2005_10