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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1666863Generated: November 1, 2026

3-Hydroxybenzaldehyde → HCID 21071620, compound

https://huagongshe.com/reaction/1666863

Reaction equation

Participants

RoleNameHCIDCharge
Reactant3-HydroxybenzaldehydeHCID 101—
ReactantWaterHCID 962—
Reactant3-ChlorophenethylamineHCID 139381—
ReactantSodium borohydrideHCID 4311764—
SolventMethanolHCID 887—
ProductHCID 21071620HCID 21071620—

Reaction Steps

Combine 2-(3-chlorophenyl)ethylamine (1.866 gm; 15.28 mmol) and 3-hydroxybenzaldehyde (1.567 gm; 10.07 mmol) in 40 mL of methanol and stir at room temperature for 20 min and treat with sodium borohydride (0.950 gm; 25.1 mmol) in one portion. Stir the mixture at room temperature. After 15 h, add water (10 mL), and remove the methanol by rotary evaporation. Add to this slurry water (25 mL) and dichloromethane (50 mL), separate the layers and extract the aqueous layer with dichloromethane (50 mL). Wash the combined organic layers with saturated brine (3×), dry over MgSO4, and concentrate to give the title compound.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08044090B2
Source datasetuspto-grants-2011_10
ORD IDord-2a15d2ab68ed4b84907b556e9874f2a0
Source noteuspto-grants-2011_10