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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1694526Generated: October 25, 2026

Trifluoroacetic acid → 5-Cyclohex-1-enyl-3-aminothiophene-2-carboxylic acid methyl ester

https://huagongshe.com/reaction/1694526

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTrifluoroacetic acidHCID 6422—
Reactant3-tert-Butoxycarbonylamino-5-(1-hydroxy-cyclohexyl)-thiophene-2-carboxylic acid methyl esterHCID 57795388—
SolventDichloromethaneHCID 6344—
Product5-Cyclohex-1-enyl-3-aminothiophene-2-carboxylic acid methyl esterHCID 5779540176.8%

Reaction Conditions

Temperature0 °C

Reaction Steps

To a solution of 3-tert-butoxycarbonylamino-5-(1-hydroxy-cyclohexyl)-thiophene-2-carboxylic acid methyl ester (68 g, 0.192 mol) in 400 mL of dichloromethane at 0° C. (ice bath) was added trifluoroacetic acid (400 mL). The mixture was stirred for 30 min at 0° C. and followed by TLC. After completion, the reaction mixture was evaporated to dryness and partitioned between ethyl acetate and saturated water solution of NaHCO3. The organic layer was separated, dried (Na2SO4) and concentrated. The residue was triturated in 4.4 volume of hexane for 30 min. Then filtered and washed with cold hexane. Dried in the vacuum oven to afford 35 g (76%) of 3-Amino-5-cyclohex-1-enyl-thiophene-2-carboxylic acid methyl ester.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08158675B2
Source datasetuspto-grants-2012_04
ORD IDord-fa4638b5eb4847cd88a5df083cc8a627
Source noteuspto-grants-2012_04