Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 15101Generated: October 26, 2026

Water → Tert.-butyl 2-[(5-bromo-thiophen-2-yl)-carbonylamino]-isobutyrate

https://huagongshe.com/reaction/15101

Reaction equation

Participants

RoleNameHCIDCharge
ReactantWaterHCID 962—
ReactantThionyl ChlorideHCID 24386—
Reactant5-Bromothiophene-2-carboxylic acidHCID 349115—
ReactantTert-butyl 2-amino-2-methylpropanoate hydrochlorideHCID 12186776—
SolventDichloromethaneHCID 6344—
ProductTert.-butyl 2-[(5-bromo-thiophen-2-yl)-carbonylamino]-isobutyrateHCID 68638345—

Reaction Steps

2.63 g (12.3 mmol) 5-bromo-thiophene-2-carboxylic acid are refluxed in 15 ml dichloromethane together with 7.0 ml of thionyl chloride for 2 h with stirring. The mixture is then evaporated down i. vac. and the residue is twice taken up in toluene and evaporated down completely i. vac. The residue is added dropwise to 10 ml dichloromethane with stirring at ambient temperature in a mixture of 2.41 g (12.3 mmol) tert.-butyl 2-amino-isobutyrate hydrochloride in 20 ml dichloromethane with 5.14 ml (36.9 mmol) TEA and stirred for 16 h. The mixture is poured into water and extracted with dichloromethane, the combined organic phases are dried over magnesium sulphate and evaporated down i. vac.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07732466B2
Source datasetuspto-grants-2010_06
ORD IDord-85ce16b4205a42c8bd3450e8ff110de5
Source noteuspto-grants-2010_06