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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 902882Generated: October 29, 2026

tert-Butanol → tert-Butyl (5-chlorothiophen-2-yl)carbamate

https://huagongshe.com/reaction/902882

Reaction equation

Participants

RoleNameHCIDCharge
Reactanttert-ButanolHCID 6386—
ReactantTriethylamineHCID 8471—
Reactant5-Chloro-2-thiophenecarboxylic acidHCID 95048—
ReactantP,P-Diphenylphosphinic azideHCID 199401—
SolventTolueneHCID 1140—
Producttert-Butyl (5-chlorothiophen-2-yl)carbamateHCID 11601095—

Reaction Conditions

Temperature80 °C

Reaction Steps

Triethylamine (1.25 ml) and diphenylphosphoryl azide (1.55 ml) were added to a suspension of 5-chlorothiophene-2-carboxylic acid (0.99 g) in toluene (20 ml), and the mixture was stirred at 80° C. for 1 hour. After the reaction mixture was cooled to room temperature, tert-butanol (2 ml) was added, and the mixture was heated under reflux for 19 hours. The reaction mixture was concentrated under reduced pressure, and methylene chloride (200 ml) was added to the resultant residue. The resultant mixture was successively washed with distilled water, a 10% aqueous solution of citric acid, distilled water, a saturated aqueous solution of sodium hydrogencarbonate and saturated aqueous solution of sodium chloride and then dried over anhydrous sodium sulfate. The solvent was distilled off under reduced pressure, and the residue was subjected to column chromatography on silica gel (hexane:ethyl acetate=4:1) to obtain tert-butyl 5-chloro-2-thienylcarbamate (1.05 g).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07365205B2
Source datasetuspto-grants-2008_04
ORD IDord-504f88c83c694042b4504fffbd637f3c
Source noteuspto-grants-2008_04