HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1939178Generated: October 30, 2026
Triethylamine → 4-(4-Nitrobenzoyl)-5,6,7,8-tetrahydro-4H-thieno[3,2-b]azepine
https://huagongshe.com/reaction/1939178
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Triethylamine | HCID 8471 | — |
| Reactant | 4-Nitrobenzoyl chloride | HCID 8502 | — |
| Reactant | 5,6,7,8-Tetrahydro-4H-thieno[3,2-B]azepine | HCID 11804971 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | 4-(4-Nitrobenzoyl)-5,6,7,8-tetrahydro-4H-thieno[3,2-b]azepine | HCID 15369398 | — |
Reaction Steps
To a solution of 10.71 g of 5,6,7,8-tetrahydro-4H-thieno[3,2-b]azepine and 19.4 ml of triethylamine amine in 150 ml of dichloromethane under argon is added in small portions 4-nitrobenzoyl chloride (exothermic). The mixture is stirred for 3 hours at 25° C. and then washed with water, sodium bicarbonate solution, brine and dried (Na2SO4). The solvent is removed, the residue dried under vacuum and recrystallized by dissolving in hot ethyl acetate and diluting with hexane. Chilling overnight and filtering gives 16 g of light brown crystals, m.p. 141°-142° C.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US05696112 |
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| Source dataset | uspto-grants-1997_12 |
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| ORD ID | ord-1d3136729df34c60a26a4eb2c9a64490 |
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| Source note | uspto-grants-1997_12 |
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