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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 539139Generated: November 2, 2026

Trifluoroacetic acid → HCID 25152743, compound

https://huagongshe.com/reaction/539139

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTrifluoroacetic acidHCID 6422—
ReactantTriethylsilaneHCID 12052—
ReactantHCID 86639580HCID 86639580—
SolventDichloromethaneHCID 6344—
ProductHCID 25152743HCID 25152743—

Reaction Steps

To a solution of 9 (24.7 mg, 0.035 mmol) in CH2Cl2 (1.4 mL) was added triethylsilane (28 μL, 0.175 mmol) followed by the dropwise addition of TFA (0.35 mL, 25% v/v). After stirring for 1 h the reaction mixture was concentrated in vacuo and put under high vacuum for 2 h to give the crude thiol 10. At 0° C. to a solution of thiol 10 in CH2Cl2 (0.45 mL) was added diisopropylethylamine (30 μL, 0.172 mmol) followed by acetyl chloride (2.43 μL, 0.034 mmol) in CH2Cl2 (0.1 mL). After stirring for 2 h 10 min 1M HCl (1 mL) was added followed by EtOAc (10 mL) the layers were separated and the organic layer was washed with sat. brine (10 mL). The organic layer was dried (MgSO4) and concentrated in vacuo. Purification by flash column chromatography (eluent 1:0-98:2-96:4-94:6-92.8 CH2Cl2/MeOH) gave the product 11 (7.3 mg, 0.014 mmol, 41%) as a white solid: Rf 0.47 MeOH/CH2Cl2 (1:9).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08865655B2
Source datasetuspto-grants-2014_10
ORD IDord-eff13ef88a504e018cc3ab26816edf0f
Source noteuspto-grants-2014_10