HuagongsheHuagongshe Chemistry Print Report · For research reference only
Triethylsilane → ethyl 7-(4-methylbenzyl)-2-(trifluoromethyl)-2H-chromene-3-carboxylate
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Triethylsilane | HCID 12052 | — |
| Reactant | ethyl 7-(4-methylbenzoyl)-2-(trifluoromethyl)-2H-chromene-3-carboxylate | HCID 69519424 | — |
| Solvent | Trifluoroacetic acid | HCID 6422 | — |
| Product | ethyl 7-(4-methylbenzyl)-2-(trifluoromethyl)-2H-chromene-3-carboxylate | HCID 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
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US07259266B2 |
| Source dataset | uspto-grants-2007_08 |
| ORD ID | ord-e53e13cc64914efbbb1312f9c6cb348b |
| Source note | uspto-grants-2007_08 |