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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1037950Generated: November 3, 2026

Triethylamine → HCID 67397491, compound

https://huagongshe.com/reaction/1037950

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTriethylamineHCID 8471—
Reactant4-(Trifluoromethyl)benzenesulfonyl chlorideHCID 2777399—
ReactantHCID 67397013HCID 67397013—
SolventDimethylformamideHCID 6228—
ProductHCID 67397491HCID 67397491—

Reaction Steps

To the vial containing (R)-tert-butyl 5-(1-aminoethyl)thiophene-2-carboxylate hydrochloride from Step 1 was added N,N-dimethylaminopyridine (3.91 mg, 0.0320 mmol), 4-(trifluoromethyl)benzenesulfonyl chloride (0.059 g, 0.24 mmol), N,N-dimethylformamide (2 mL), and triethylamine (0.178 mL, 1.28 mmol). The mixture was stirred at rt for 16 h and then evaporated. To the residue was added 1,2-dichloroethane (3 mL), sat. NaHCO3 solution (0.5 mL), and water (0.5 mL). After separation, the aqueous layer was extracted with 1,2-dichloroethane (2×3 mL). The combined organic phases were evaporated to dryness to give crude (R)-tert-butyl 5-(1-(4-(trifluoromethyl)phenylsulfonamido)ethyl)thiophene-2-carboxylate as a brown solid. LC-MS: (FA) ES− 434.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08546588B2
Source datasetuspto-grants-2013_10
ORD IDord-2a85f760e26b48b389213b84bda85279
Source noteuspto-grants-2013_10