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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 482077Generated: October 26, 2026

Acetylresorcinol → 3-Benzyloxyphenyl acetate

https://huagongshe.com/reaction/482077

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAcetylresorcinolHCID 5055—
ReactantBenzyl BromideHCID 7498—
ReactantSodium hydrideHCID 24758—
SolventDimethylformamideHCID 6228—
Product3-Benzyloxyphenyl acetateHCID 2234586555%

Reaction Steps

Resorcinol monoacetate (6.10 g, 40 mmol) in DMF (10 mL) was added dropwise to a mixture of NaH (95%, 0.92 g, 40 mmol) in DMF (50 mL). The reaction mixture was stirred at room temperature for 10 min. Benzyl bromide (6.85 g, 40 mmol) in DMF (10 mL) was added dropwise and stirring was continued at room temperature for 2 h. The reaction was quenched carefully with water (100 mL) and then extracted with ethyl acetate (3×100 mL). The organic phase was washed with brine (2×50 mL), dried over Na2 SO4, and concentrated in vacuo. The residue was then purified by flash column chromatography (1:1 hexane:methylene chloride) to give the title compound as a white solid (5.30 g, 55%). 1H-NMR (300 MHz, CDCl3) δ 2.28 (s, 3H), 5.03 (s, 2H), 6.72 (m, 2H), 6.85 (dd, 1H), 7.27 (t, 1H), 7.41 (m, 5H).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05792769
Source datasetuspto-grants-1998_08
ORD IDord-7c40cba6b854474296734844174ab641
Source noteuspto-grants-1998_08