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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 580981Generated: October 25, 2026

Water → 4-Allyloxyphenylmethyloxy acetate

https://huagongshe.com/reaction/580981

Reaction equation

Participants

RoleNameHCIDCharge
ReactantWaterHCID 962—
ReactantMethyl chloroacetateHCID 7295—
ReactantSodium hydrideHCID 24758—
Reactant(4-(Prop-2-en-1-yloxy)phenyl)methanolHCID 11744970—
SolventDimethylformamideHCID 6228—
Product4-Allyloxyphenylmethyloxy acetateHCID 8675416238.9%

Reaction Steps

Sodium hydride (1.20 g; 60% dispersion in oil) was added over a period of 10 minutes to a stirred solution of 4-allyloxybenzyl alcohol (4.60 g) in DHF (20 ml) at 0° C. under an atmosphere of argon. After 0.5 hours, a solution of methylchloroacetate (3.30 g) in DMF (10 ml) was added over a period of 0.25 hours. The reaction mixture was stirred for 40 hours at ambient temperature. Water (300 ml) was added and the mixture extracted with ethyl acetate (3×100 ml). The ethyl acetate extracts were combined, washed with brine (2×100 ml), dried (MgSO4) and evaporated. The residue was purified by flash column chromatography on silica gel using a 9:1 (v/v) mixture of hexane/ethyl acetate to give 4-allyloxyphenylmethyloxy acetate (2.42 g) as a colourless oil; NMR(CDCl3): 3.75(3H,s), 4.07(2H,s), 4.52(4H,m), 5.36(2H,m), 6.10(1H,m), 6.88(2H,m) and 7.28(2H,m); m/z 236(H).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05919793
Source datasetuspto-grants-1999_07
ORD IDord-aa7a3fa4f1004114a4fed55e8f77e892
Source noteuspto-grants-1999_07