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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1968971Generated: October 30, 2026

Sodium Hydroxide → 1-Methyl-4-(2-methoxyethoxy)cyclohexanecarboxylic acid

https://huagongshe.com/reaction/1968971

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSodium HydroxideHCID 14798—
ReactantIsobutyl 1-methyl-4-(2-methoxyethoxy)cyclohexanecarboxylateHCID 59444164—
Solvent1,4-DioxaneHCID 31275—
Product1-Methyl-4-(2-methoxyethoxy)cyclohexanecarboxylic acidHCID 59444069—

Reaction Conditions

Temperature100 °C

Reaction Steps

A mixture of isobutyl 1-methyl-4-(2-methoxyethoxy)cyclohexanecarboxylate (D68, 27 g, 49.6 mmol), 1,4-dioxane (100 mL) and 3M aqueous sodium hydroxide (100 mL, 300 mmol) was heated at 100° C. for 18 h then cooled and partitioned between water and diethyl ether. The aqueous phase was acidified and extracted with ethyl acetate to give the desired product. Unreacted starting material remained in the ether wash, so the ether was evaporated and the residue dissolved in a mixture of THF (100 mL), methanol (100 mL), and 6M aqueous sodium hydroxide (100 mL) and heated at 65° C. for 18 h then worked up as before to give additional product, which was combined to give 1-methyl-4-(2-methoxyethoxy)cyclohexanecarboxylic acid (9.5 g, 43.9 mmol, 89% yield) as a pale yellow oil.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08426443B2
Source datasetuspto-grants-2013_04
ORD IDord-4a19e185538241e4a1315b843135cce9
Source noteuspto-grants-2013_04