HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 482077Generated: October 26, 2026
Acetylresorcinol → 3-Benzyloxyphenyl acetate
https://huagongshe.com/reaction/482077
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Acetylresorcinol | HCID 5055 | — |
| Reactant | Benzyl Bromide | HCID 7498 | — |
| Reactant | Sodium hydride | HCID 24758 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Product | 3-Benzyloxyphenyl acetate | HCID 22345865 | 55% |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US05792769 |
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| Source dataset | uspto-grants-1998_08 |
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| ORD ID | ord-7c40cba6b854474296734844174ab641 |
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| Source note | uspto-grants-1998_08 |
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