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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1190049Generated: October 30, 2026

Trifluoroacetic acid → HCID 178499306, compound

https://huagongshe.com/reaction/1190049

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTrifluoroacetic acidHCID 6422—
ReactantTriethylsilaneHCID 12052—
ReactantSodium BicarbonateHCID 516892—
ReactantHCID 178499309HCID 178499309—
SolventDichloromethaneHCID 6344—
ProductHCID 178499306HCID 17849930645.7%

Reaction Steps

A solution of 5-(1-hydroxy-cyclohex-2-enyl)-3-{(trans-4-methyl-cyclohexanecarbonyl)-[trans-4-(tetrahydro-pyran-2-yloxy)-cyclohexyl]-amino}-thiophene-2-carboxylic acid methyl ester (48 mg, 0.086 mmol) in DCM (1 mL) was cooled to −50° C. Triethylsilane (43 μl, 0.27 mmol) was added followed by gradual addition of trifluoroacetic acid (total 22 μl, 0.28 mmol) (4 μl to 6 μl every 30 min). The mixture was stirred at −40° C. to −50° C. for 3.5 h. Aqueous NaHCO3 was added and the mixture was allowed to come to room temperature. It was extracted with DCM, washed with brine, dried (MgSO4) and evaporated. The crude was left at room temperature for 2 days and purified by chromatography over silica gel (hexane-EtOAc mixtures) yielding 5-(3-Hydroxy-cyclohex-1-enyl)-3-{(trans-4-methyl-cyclohexanecarbonyl)-[trans-4-(tetrahydro-pyran-2-yloxy)-cyclohexyl]-amino}-thiophene-2-carboxylic acid methyl ester (22 mg, 45%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08674118B2
Source datasetuspto-grants-2014_03
ORD IDord-98ae2cb020c94b9eb115168b81201aaa
Source noteuspto-grants-2014_03