HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1365603Generated: November 2, 2026
Aluminum(III) Chloride → 4,5,7,8-Tetrahydro-thieno[2,3-d]azepine-6-carboxylic acid ethyl ester
https://huagongshe.com/reaction/1365603
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Aluminum(III) Chloride | HCID 6451240 | — |
| Reactant | 4-Oxo-4,5,7,8-tetrahydro-thieno[2,3-d]azepine-6-carboxylic acid ethyl ester | HCID 57423983 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | 4,5,7,8-Tetrahydro-thieno[2,3-d]azepine-6-carboxylic acid ethyl ester | HCID 59302541 | 65% |
Reaction Steps
AlCl3 (3.95 g, 29.7 mmol) was added to 50 mL DCM at 0° C. Borane-t-butyl amine complex (5.2 g, 59.5 mmol) was added followed by the product of step (c) (2.37 g, 9.9 mmol) dissolved in DCM (50 mL). The reaction was stirred for 2 hours at room temperature after which time another 3.95 g (29.7 mmol) of AlCl3 was added. After stirring for 10 minutes, the reaction was quenched carefully with 0.1 M HCl (˜50 mL). After concentration of the organic solvent, the crude reaction mixture was partitioned between 1M HCl and EtOAc (70 mL each). The aqueous layer was back extracted 1× EtOAc. The combined organic layers were dried over MgSO4 and concentrated. The sub-title product (1.45 g) was obtained after purification by silica gel chromatography (0 to 35% EtOAc in Hexanes). MS: ESI (positive): 226 (M+H).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07893051B2 |
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| Source dataset | uspto-grants-2011_02 |
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| ORD ID | ord-ad033a5fc71447e79d0b03ebec71d72a |
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| Source note | uspto-grants-2011_02 |
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