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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 854882Generated: October 29, 2026

Triethylsilane → ethyl 7-(4-methylbenzyl)-2-(trifluoromethyl)-2H-chromene-3-carboxylate

https://huagongshe.com/reaction/854882

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTriethylsilaneHCID 12052—
Reactantethyl 7-(4-methylbenzoyl)-2-(trifluoromethyl)-2H-chromene-3-carboxylateHCID 69519424—
SolventTrifluoroacetic acidHCID 6422—
Productethyl 7-(4-methylbenzyl)-2-(trifluoromethyl)-2H-chromene-3-carboxylateHCID 69517327—

Reaction Steps

The ester from Step 1 was dissolved in TFA (18 mL). Et3SiH was added dropwise at room temperature. The reaction was stirred at room temperature overnight. The reaction was quenched with NaHCO3 and extracted with ether. The organic layer was dried over MgSO4. The filtrate was concentracted to give yellow oil, which was purified by Biotage with 3-5% EtOAc in hexane to give clear oil quantity: LCMS m/z 377.15 (M+H). 1H NMR (CDCl3/400 MHz) 7.68 (s, 1H), 7.08 (m, 4H), 6.79 (d, 1H, J=6.4 Hz), 5.68 (q, 1H, J=7.2 Hz), 4.29 (m, 2H), 3.89 (s, 2H), 2.31 (s, 3H), 1.35 (t, 3H, J=7.2 Hz).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07259266B2
Source datasetuspto-grants-2007_08
ORD IDord-e53e13cc64914efbbb1312f9c6cb348b
Source noteuspto-grants-2007_08