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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 488268Generated: October 29, 2026

Sodium Hydroxide → 3-(Octadecyloxy)-5-(phenylmethoxy)benzoic acid

https://huagongshe.com/reaction/488268

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSodium HydroxideHCID 14798—
Reactant3-(Octadecyloxy)-5-(phenylmethoxy)benzoic acid methyl esterHCID 54033513—
SolventMethanolHCID 887—
Solvent1,4-DioxaneHCID 31275—
Product3-(Octadecyloxy)-5-(phenylmethoxy)benzoic acidHCID 1938904688.5%

Reaction Steps

A mixture of 3.0 g (7.1 mmol) of 3-hydroxy-5-(octadecyloxy) benzoic acid methyl ester, 0.93 ml (7.85 mmol) of benzyl bromide and 2.0 g (14.5 mmol) of potassium carbonate in 50 ml of DMF was stirred at 85° for 50 hours. The solvent was removed at reduced pressure and the residue was extracted with methylene chloride. The extract was concentrated and recrystallized from methylene chloride-methanol to give 3.24 g (89% yield, mp 62°-64°) of 3-(octadecyloxy)-5-(phenylmethoxy)benzoic acid methyl ester. A solution of 3.24 g (6.3 mmol) of 3-(octadecyloxy)-5-(phenylmethoxy) benzoic acid methyl ester and 3 ml (18 mmol) of 6N NaOH in 100 ml of methanol and 25 ml of dioxane was stirred at reflux for 3.5 hours. The solvents were removed at reduced pressure and the residue was acidified and extracted with ethyl acetate. The dried extract was concentrated to a solid which was recrystallized from methylene chloride-hexane to give 2.77 g (88% yield, mp 101°-103°) of 3-(octadecyloxy)-5-(phenylmethoxy)benzoic acid.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05298652
Source datasetuspto-grants-1994_03
ORD IDord-efbc7d945bff479d813f1ddb0ef6639e
Source noteuspto-grants-1994_03