HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 519354Generated: October 26, 2026
Tert-Butylamine → N-tert-Butyl-4,5,6,7-tetrahydrobenzo[b]thiophene-2-carboxamide
https://huagongshe.com/reaction/519354
Participants
| Role | Name | HCID | Charge |
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| Reactant | Tert-Butylamine | HCID 6385 | — |
| Reactant | Thionyl Chloride | HCID 24386 | — |
| Reactant | 4,5,6,7-Tetrahydro-1-benzothiophene-2-carboxylic acid | HCID 2063443 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | N-tert-Butyl-4,5,6,7-tetrahydrobenzo[b]thiophene-2-carboxamide | HCID 4806824 | 88.9% |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US09115152B2 |
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| Source dataset | uspto-grants-2015_08 |
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| ORD ID | ord-b31b74845a2d4412b0ecf0e3629299d5 |
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| Source note | uspto-grants-2015_08 |
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