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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1787920Generated: October 30, 2026

Carbon Dioxide → 4-Isopropyl-2-(methoxymethoxy)benzyl Alcohol

https://huagongshe.com/reaction/1787920

Reaction equation

Participants

RoleNameHCIDCharge
ReactantCarbon DioxideHCID 280—
Reactant4-MethylmorpholineHCID 7972—
ReactantEthyl chloroformateHCID 10928—
ReactantSodium borohydrideHCID 4311764—
Reactant4-Isopropyl-2-methoxymethoxybenzoic acidHCID 68532278—
SolventMethanolHCID 887—
SolventTetrahydrofuranHCID 8028—
Product4-Isopropyl-2-(methoxymethoxy)benzyl AlcoholHCID 5760245950%

Reaction Conditions

Temperature-10 °C

Reaction Steps

To a solution of 4-isopropyl-2-(methoxymethoxy)benzoic acid, which may be prepared as described in Exmple 6-B, (2.40 g, 11.0 mmol) and 4-methylmorpholine (1.18 mL, 11.0 mmol) in 50 mL dry tetrahydrofuran at −10° C. was added dropwise ethyl chloroformate (1.02 mL, 11.0 mmol). After stirring at −10° C. for 20 min, sodium borohydride (1.21 g, 33.0 mmol) was added all at once. Methanol (150 mL) was cautiously added dropwise. Once the vigorous evolution of carbon dioxide had significantly decreased, the remaining methanol was added. Stirring was continued for 30 min, and the reaction was quenched with 10% acetic acid in water. The volatile solvents were removed, and the remaining material was diluted with ether. The ether was extracted with saturated NaHCO3 (2×), water (2×), brine (1×), and dried over MgSO4. The crude material was purified by chromatography over silica, using an eluent gradient of 10-30% ethyl acetate in hexanes, to afford the alcohol (1.16 g, 50%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07511066B2
Source datasetuspto-grants-2009_03
ORD IDord-dff22854df074758802314edeec71394
Source noteuspto-grants-2009_03