HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2403737Generated: October 26, 2026
Boron trifluoride etherate → 4-(5-Bromo-2-chlorobenzyl)phenethyl acetate
https://huagongshe.com/reaction/2403737
Participants
| Role | Name | HCID | Charge |
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| Reactant | Boron trifluoride etherate | HCID 8000 | — |
| Reactant | Triethylsilane | HCID 12052 | — |
| Reactant | 4-(5-Bromo-2-chlorobenzoyl)phenethyl acetate | HCID 59557742 | — |
| Product | 4-(5-Bromo-2-chlorobenzyl)phenethyl acetate | HCID 59557787 | 65% |
Reaction Steps
A mixture of 4-(5-bromo-2-chlorobenzoyl)phenethyl acetate (intermediate BF) (1 g, 2.62 mmol), borontrifluoride diethylether (0.65 mL, 10.4 mmol) and triethylsilane (0.84 mL, 10.4 mmol) was heated at 85° C. for 2 h in a sealed tube. The reaction vessel was cooled to room temperature and ice-water (50 mL) was added. The product was extracted with ethyl acetate (2×25 mL), washed with brine (25 mL), dried (Na2SO4), filtered and evaporated. Purification on silica gel using an ISCO column with 5% ethyl acetate in hexane gave intermediate BG (620 mg, yield 65%). 1H NMR (300 MHz, CDCl3): δ 7.27-7.10 (m, 7H), 4.27 (t, J=6.9, 7.2 Hz, 2H), 4.03 (s, 2H), 2.92 (t, J=6.9, 7.2 Hz, 2H), 2.05 (s, 3H.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08802637B2 |
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| Source dataset | uspto-grants-2014_08 |
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| ORD ID | ord-5619c793660d4473a4c9fa0a6f84db42 |
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| Source note | uspto-grants-2014_08 |
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