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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 324885Generated: October 31, 2026

Benzyl Bromide → HCID 22005268, compound

https://huagongshe.com/reaction/324885

Reaction equation

Participants

RoleNameHCIDCharge
ReactantBenzyl BromideHCID 7498—
ReactantPotassium CarbonateHCID 11430—
ReactantHCID 22004934HCID 22004934—
SolventAcetoneHCID 180—
SolventAmmonium ChlorideHCID 25517—
ProductHCID 22005268HCID 22005268100%

Reaction Steps

A mixture of the racemic compound prepared in Example 241 (293 mg, 851 μmol), benzyl bromide (110 μL, 925 μmol), and potassium carbonate (303 mg, 2.19 mmol) in acetone (29 mL) was heated to reflux for 3 h. The mixture was diluted with saturated aqueous ammonium chloride solution (50 mL) and extracted with Et2O (3×50 mL). Silica gel chromatography (90:10 hexane/ethyl acetate) provided a colorless oil (0.369 g, 100%). 1H NMR (CDCl3, 300 MHz): δ 7.34 (s, 1H), 7.23 (m, 3H), 7.12 (m, 1H), 7.03 (m, 2H), 6.84-6.75 (m, 2H), 5.04 (d, 12.1 Hz, 1H), 4.94 (d, 12.1 Hz, 1H), 4.38 (dd, 11.4 Hz, 8.5 Hz, 1H), 4.25 (dd, 11.4 Hz, 3.3 Hz, 1H), 3.39 (sept, 6.9 Hz, 1H), 3.18 (sept, 6.9 Hz, 1H), 2.30-2.40 (m, 1H), 2.09-2.20 (m, 1H), 1.65 (dd, 8.5 Hz, 3.3 Hz, 1H), 1.26-1.34 (m, 14H), 0.72 (t, 7.4 Hz, 3H).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06218431B1
Source datasetuspto-grants-2001_04
ORD IDord-a851cede302946cca4f4063c36b3ea0c
Source noteuspto-grants-2001_04