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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 964871Generated: October 30, 2026

Sodium Hydroxide → 3-Allyloxy-benzoic acid

https://huagongshe.com/reaction/964871

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSodium HydroxideHCID 14798—
ReactantSodium BisulfateHCID 516919—
ReactantHCID 11321926HCID 11321926—
SolventMethanol--water (1/1)HCID 22242641—
Product3-Allyloxy-benzoic acidHCID 648388497.8%

Reaction Steps

A solution of 917 mg (4.2 mmol) of 3-(2-propenyloxy)benzoic acid, 2-propenyl ester in 9 mL of methanol/water (3:2) at room temperature is treated with 0.53 mL (5.25 mmol) of 10M sodium hydroxide solution. The solution is allowed to stir for one hour then acidified with 5 mL of 10% sodium bisulfate solution and extracted with 25 mL of ethyl acetate. The organic layer is washed with saturated sodium chloride solution, dried over magnesium sulfate, and concentrated in vacuo to give 732 mg (97%) of 3-(2-propenyloxy)benzoic acid as a white powder. The product is utilized in the next reaction without further purification; m.p. 78°-79°; the 1H NMR (300 MHz, CDCl3) is consistent with the desired product; IR (KBr) 3000, 1690, 1620, 1590 cm-1 ; MS (CI low res) m/e 179 (M+H), 161, 135; Analysis calculated for C10H10O3 : C, 67.41; H, 5.66; found: C, 67.37; H, 5.59.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05773001
Source datasetuspto-grants-1998_06
ORD IDord-fd62647bd8d34f6c8788a2813a470c81
Source noteuspto-grants-1998_06