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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1843227Generated: November 2, 2026

Tert-Butylamine → N-tert-Butyl-4,5,6,7-tetrahydrobenzo[b]thiophene-2-carboxamide

https://huagongshe.com/reaction/1843227

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTert-ButylamineHCID 6385—
ReactantThionyl ChlorideHCID 24386—
Reactant4,5,6,7-Tetrahydro-1-benzothiophene-2-carboxylic acidHCID 2063443—
SolventDichloromethaneHCID 6344—
ProductN-tert-Butyl-4,5,6,7-tetrahydrobenzo[b]thiophene-2-carboxamideHCID 480682488.9%

Reaction Steps

A mixture of 4,5,6,7-tetrahydrobenzo[b]thiophene-2-carboxylic acid (500 g, 2.75 mol, 1.0 equiv) and thionyl chloride (655 g, 5.5 mol, 2.0 equiv) was boiled under reflux for 3 h. Excess thionyl chloride was removed by distillation under reduced pressure. The residue was taken up in dichloromethane (1.0 L) and a solution of tert-butylamine (402 g, 5.5 mol, 2.0 equiv) in dichloromethane (500 mL) was added with stirring while the temperature of the mixture was kept below 10° C. The resulting solution was stirred at 25° C. for 16 h. Most of the solvent was removed under reduced pressure. The residue was chilled in an ice-bath and 2M KOH solution was introduced slowly to adjust the pH to 11 with stirring. The suspension was filtered and the solid was collected, washed three times with water, and dried in vacuo to afford 117a as a white solid (580 g, 80%, over two steps). MS: [M+H]+ 238. 1H NMR (500 MHz, CDCl3) δ 7.02 (s, 1H), 5.77 (s, 1H), 2.65 (t, J=6.0 Hz, 1H), 2.47 (t, J=6.0 Hz, 1H), 1.74-1.70 (m, 4H), 1.35 (s, 9H).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08946213B2
Source datasetuspto-grants-2015_02
ORD IDord-97c33ffce28249369aa65889f452f8b8
Source noteuspto-grants-2015_02