Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 575030Generated: October 30, 2026

Triethylsilane → HCID 86693062, compound

https://huagongshe.com/reaction/575030

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTriethylsilaneHCID 12052—
ReactantHCID 86693061HCID 86693061—
SolventTrifluoroacetic acidHCID 6422—
ProductHCID 86693062HCID 8669306274.1%

Reaction Steps

Into a 1000-mL round-bottom flask was placed a solution of 3-(4-bromo-3-fluorophenyl)-3-hydroxycyclobutane-1-carboxylic acid (50 g, 172.95 mmol, 1.00 equiv) in trifluoroacetic acid (500 mL) and triethylsilane (40.1 g, 344.87 mmol, 2.00 equiv). The resulting solution was stirred at room temperature for 4 h and concentrated under vacuum. The resulting solution was diluted with 200 mL of EA and washed with 2×200 mL of saturated aqueous sodium carbonate. The aqueous layers were combined and extracted with 3×500 mL of EA. The pH value of the aqueous layer was adjusted to 4 with hydrogen chloride (1 mol/L). The resulting solution was extracted with 3×500 mL of ethyl acetate. The organic layers were combined, washed with 1×1000 mL of water and 1)(1000 mL of brine, dried over anhydrous sodium sulfate and concentrated under vacuum to afford 35 g (crude) of 3-(4-bromo-3-fluorophenyl)cyclobutane-1-carboxylic acid as a yellow liquid.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09034866B2
Source datasetuspto-grants-2015_05
ORD IDord-33227d2523894a07a45739b234d33b75
Source noteuspto-grants-2015_05