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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 38631Generated: October 26, 2026

Acetovanillone → 2',3'-Dihydroxyacetophenone

https://huagongshe.com/reaction/38631

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAcetovanilloneHCID 2214—
ReactantBenzyl BromideHCID 7498—
ReactantPotassium CarbonateHCID 11430—
SolventAcetonitrileHCID 6342—
Product2',3'-DihydroxyacetophenoneHCID 642911070.3%

Reaction Conditions

Temperature25 °C

Reaction Steps

To a solution of acetovanillone (33) (4.70 g, 28.3 mmol) in MeCN (60 mL) was added K2CO3 (8.05 g, 58.3 mmol) and KI (0.20 g, 1.2 mmol). The mixture was stirred under N2 atmosphere and benzyl bromide (34) (4.0 mL, 34 mmol) was added dropwise. The reaction mixture was reflux for 24 h and then cooled to 25° C., then resulting precipitate was filtered off. The filtrate was evaporated and purified by column chromatography (SiO2, n-hexane: CH2Cl2=1:2) to give 30. White solid; yield: 70.3%; mp 87-88° C.; 1H-NMR (CDCl3. 200 MHz): δ 2.51 (s, 3H), 3.91 (s, 3H), 5.20 (s, 2H), 6.86 (d, J=8.2 Hz, 1H), 7.21-7.55 (m, 7H); 13C-NMR (CDCl3, 50 MHz): δ 26.19, 56.05, 70.79, 110.53, 112.13, 123.07, 127.18, 128.10, 128.68, 130.72, 136.28, 149.49, 152.41, 196.80; Anal. calcd for C16H16O3: C, 74.98; H, 6.29. Found: C, 75.02; H, 6.25.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08524740B2
Source datasetuspto-grants-2013_09
ORD IDord-904a19f9ad764a429ae73edd9fd181c0
Source noteuspto-grants-2013_09