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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

Reaction equation

Participants

RoleNameHCIDCharge
Reactant2-(2-Bromoethylthio)-thiopheneHCID 12201119—
ReactantHCID 178501207HCID 178501207—
SolventAcetonitrileHCID 6342—
ProductHCID 178501227HCID 17850122772%

Reaction Conditions

Temperature100 °C

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

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09133219B2
Source datasetuspto-grants-2015_09
ORD IDord-5b8839e0f36d467c9a80375019dc5a1a
Source noteuspto-grants-2015_09