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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 990113Generated: October 30, 2026

3-Methoxy-4-propoxybenzaldehyde → (3-Methoxy-4-propoxyphenyl)methanol

https://huagongshe.com/reaction/990113

Reaction equation

Participants

RoleNameHCIDCharge
Reactant3-Methoxy-4-propoxybenzaldehydeHCID 592110—
ReactantSodium borohydrideHCID 4311764—
SolventEthanolHCID 702—
Product(3-Methoxy-4-propoxyphenyl)methanolHCID 212529892.4%

Reaction Conditions

Temperature0 °C

Reaction Steps

Crude 4-(propyloxy)-3-methoxybenzaldehyde (2.55 g) was dissolved in EtOH (30 mL) and cooled to 0° C. NaBH4 (0.499 g, 13.2 mmol) was added portionwise. After the addition was completed, the ice-water bath was removed and the reaction mixture was stirred at room temperature for 2 hours. Water (50 mL) was added and the resulting mixture was extracted with diethyl ether (3×100 mL). The combined organic layers were dried over anhydrous MgSO4. Removal of the solvent gave a pale yellow oil which was purified by silica gel column chromatography (hexanes/EtOAc, 4:1) to give 4-(propyloxy)-3-methoxybenzyl alcohol (2.38 g, 92% over two steps) as a colorless oil.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06458829B1
Source datasetuspto-grants-2002_10
ORD IDord-bdd824bc7fe94e85924d95570dae0ec8
Source noteuspto-grants-2002_10