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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1810695Generated: November 3, 2026

Dichloromethane → (e)-3-[4-(3-Dimethylamino-prop-1-ynyl)-phenyl]-3-phenylprop-2-en-1-ol

https://huagongshe.com/reaction/1810695

Reaction equation

Participants

RoleNameHCIDCharge
ReactantDichloromethaneHCID 6344—
ReactantAmmonium ChlorideHCID 25517—
ReactantDiisobutylaluminumhydrideHCID 21225700—
Reactant(E)-3-[4-(3-dimethylamino-prop-1-ynyl)-phenyl]-3-phenyl-acrylic acid ethyl esterHCID 67145970—
SolventTetrahydrofuranHCID 8028—
Product(e)-3-[4-(3-Dimethylamino-prop-1-ynyl)-phenyl]-3-phenylprop-2-en-1-olHCID 67145875—

Reaction Steps

A 1 M solution of diisobutylaluminum hydride in tetrahydrofuran (6 ml) was added drop wise to a cooled (0° C.) solution of the above ester (0.600 g; 1.80 mmol) in dry tetrahydrofuran (50 ml). The reaction stirred at the temperature for 4 hours and then added saturated ammoniumchloride (30 ml). After stirring 30 min dichloromethane (150 ml) and hyflo super cell medium (15 g) were added. The mixture was stirred at ambient temperature 2 hours, filtered and evaporated in vacuo. The crude product was taken up in dichloromethane (150 ml) and washed with water (2×50 ml), dried with anhydrous magnesium sulfate and subsequently evaporated in vacuo giving (E)-3-[4-(3-dimethylamino-prop-1-ynyl)-phenyl]-3-phenyl-prop-2-en-1-ol.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08362016B2
Source datasetuspto-grants-2013_01
ORD IDord-d9b3feaec1664d75a1afff5fd6ec2c68
Source noteuspto-grants-2013_01