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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 568970Generated: October 31, 2026

Hydrochloric Acid → 3-(Benzyloxy)propanal

https://huagongshe.com/reaction/568970

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydrochloric AcidHCID 313—
ReactantDimethyl SulfoxideHCID 679—
ReactantOxalyl chlorideHCID 65578—
Reactant3-Benzyloxy-1-propanolHCID 347971—
SolventDichloromethaneHCID 6344—
SolventTriethylamineHCID 8471—
Product3-(Benzyloxy)propanalHCID 10888261—

Reaction Conditions

Temperature-50 °C

Reaction Steps

Under nitrogen, a solution of DMSO (8.4 mL, 118 mmoles) in dry dichloromethane (125 mL) is cooled to -60° C., and oxalyl chloride (5 mL, 59 mmoles) in CH2Cl2 (40 mL) is added slowly. After stirring for 5 min at -50° C., 3-benzyloxy-1-propanol (14), 8.9 g, 53.7 mmoles) in CH2Cl2 (27 mL) is added at -60° C. Stirring is continued for 15 min, then triethylamine (47 mL) is added slowly at -60° C. After 5 min at this temperature, the mixture is allowed to warm up to room temperature. After addition of 0.5N HCl and phase separation, the organic phase is washed with water until neutral. Drying (Na2SO4) and evaporation gives the crude aldehyde as an oil: 10.6 g. Distillation under vacuum gives pure 15: 6.54 g (74%), bp 170° C. (15 mm Hg).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04730006
Source datasetuspto-grants-1988_03
ORD IDord-a21bbec554da42dc89907fe23201e65d
Source noteuspto-grants-1988_03