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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 369511Generated: October 31, 2026

Benzyl Bromide → HCID 10549342, compound

https://huagongshe.com/reaction/369511

Reaction equation

Participants

RoleNameHCIDCharge
ReactantBenzyl BromideHCID 7498—
ReactantPotassium CarbonateHCID 11430—
ReactantHCID 383045HCID 383045—
SolventEthanolHCID 702—
ProductHCID 10549342HCID 10549342109.7%

Reaction Conditions

Temperature100 °C

Reaction Steps

Benzyl bromide (4.5 g, 38 mmol) was added to a suspension of 2-ethoxy-β-estra-3,17β-diol (2) (4.5 g, 13 mmol) and potassium carbonate (8.6 g, 62 mmol) in anhydrous ethanol (100 mL) under argon atmosphere at 0° C. The resulting mixture was stirred at 100±5° C. for 7-8 h. The solvent was evaporated under reduced pressure and the residue was diluted with water, and the mixture was extracted with ethyl acetate (3×200 mL). The combined organic solution was washed with water (100 mL), sodium bicarbonate (120 mL), brine (100 mL), and dried over sodium sulfate. The ethyl acetate layer on evaporation under reduced pressure gave a viscous oil (5.8 g), which was used as such without any further purification in the next step: 1H NMR, (CDCl3) δ 7.35 (s, 5 H), 6.75 (s, 1 H) 6.65 (s, 1 H), 5.5 (s, 1 H), 4.55 (s, 2 H), 4.04 (q, J=6.4, 2 H), 3.5 (t, J=8.5 Hz, 1 H), 2.75 (m, 3 H), 2.20-1.95 (m, 6 H), 1.90-1.80 (m, 2 H), 1.75-1.5 (m, 2 H), 1.45-1.1 (m, 7 H, 0.85 (s, 1 H).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06136992
Source datasetuspto-grants-2000_10
ORD IDord-3d90430eff70488ea9f921e7cd22ba82
Source noteuspto-grants-2000_10