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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2256776Generated: October 31, 2026

Sodium Hydroxide → HCID 19027302, compound

https://huagongshe.com/reaction/2256776

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSodium HydroxideHCID 14798—
Reactant4-(2-{2-[(Prop-2-en-1-yl)oxy]ethoxy}ethoxy)benzoic acidHCID 19027288—
ReactantMethyl 4-(2-{2-[(prop-2-en-1-yl)oxy]ethoxy}ethoxy)benzoateHCID 19027301—
SolventMethanolHCID 887—
ProductHCID 19027302HCID 1902730294.3%

Reaction Conditions

Temperature0 °C

Reaction Steps

These compounds were synthesized by similar methods. The representative synthesis of 4-(2-(2-allyloxyethoxy)ethoxy)benzoic acid (11) is presented. A mixture of 8.39 grams (0.03 mole) of the obtained methyl 4-(2-(2-allyloxy-ethoxy)ethoxy)benzoate (7), 6 ml of 50% aqueous sodium hydroxide solution and 150 ml of methanol was stirred under reflux for three hours. Methanol was distilled off (100 ml) and water 600 ml was added. The reaction mixture was acidified with hydrochloric acid. After cooling to 0° C., a white solid was filtered and set aside. The filtrate was extracted with dichloromethane and the extracted material was evaporated to a white solid which was combined with the set-aside material. The combined material was dried under vacuum to yield 4.4 g of product (94.3%). 1H-NMR (CDCl3, TMS): d=3.81-4.25 (m, 10H, --CH2 --(OCH2CH2)2 -- ), 5.23 and 5.9 (m, 3H, CH2 =CH--), 6.95 and 8.05 (2d, 4 aromatic protons), 12.2 (s, 1H, --COOH).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05656197
Source datasetuspto-grants-1997_08
ORD IDord-3ac563d5d9934382807ed3baa13b2fd9
Source noteuspto-grants-1997_08