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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1707919Generated: October 31, 2026

Methanol → HCID 18960339, compound

https://huagongshe.com/reaction/1707919

Reaction equation

Participants

RoleNameHCIDCharge
ReactantMethanolHCID 887—
ReactantTolueneHCID 1140—
ReactantPhenoxyethanolHCID 31236—
ReactantPotassium bisulfateHCID 516920—
ReactantHCID 18960338HCID 18960338—
ProductHCID 18960339HCID 18960339—

Reaction Steps

A mixture of 2 g (7.45 mmol) of 4-(tert.-butoxycarbonyloxy)-benzaldehyde dimethylacetal, 2.06 g (14.9 mmol) of 2-phenoxyethanol and 40 mg of potassium hydrogensulfate was heated to the boil in 30 ml of dried toluene under a reflux condenser. After heating for 1 hour, the methanol formed was distilled off slowly, while more toluene was added to the mixture. After complete removal of the methanol, the mixture was cooled down, the potassium hydrogen sulfate catalyst was filtered off and the toluene was stripped off. The oily residue was dissolved in dichloromethane and washed with water. The organic phase was dried over magnesium sulfate. After the solvent had been stripped off under reduced pressure, the product was dried in an oil pump vacuum.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05356752
Source datasetuspto-grants-1994_10
ORD IDord-9ff583a7b94347ae89c9dbccde130a47
Source noteuspto-grants-1994_10