HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2279338Generated: October 30, 2026
2-(2-Bromoethylthio)-thiophene → HCID 178501227, compound
https://huagongshe.com/reaction/2279338
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | 2-(2-Bromoethylthio)-thiophene | HCID 12201119 | — |
| Reactant | HCID 178501207 | HCID 178501207 | — |
| Solvent | Acetonitrile | HCID 6342 | — |
| Product | HCID 178501227 | HCID 178501227 | 72% |
Reaction Steps
2-(2-Bromo-ethylsulfanyl)-thiophene (275 mg, 1.21 mmol, 1.0 eq) is added at room temperature to a stirred solution of trans-4-amino-cyclohexanecarboxylic acid methyl ester (200 mg, 1.21 mmol, 1.0 eq) in acetonitrile (6 mL). After 15 hours stirring at 100° C., the reaction mixture is evaporated to afford trans-4-[2-(thiophen-2-ylsulfanyl)-ethylamino]-cyclohexanecarboxylic acid methyl ester as an off-white oil (261 mg, 68% yield).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US09133219B2 |
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| Source dataset | uspto-grants-2015_09 |
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| ORD ID | ord-5b8839e0f36d467c9a80375019dc5a1a |
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| Source note | uspto-grants-2015_09 |
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