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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 247696Generated: October 27, 2026

Acetone → 1,3-Propanediol, 2-(4-pentenyl)-

https://huagongshe.com/reaction/247696

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAcetoneHCID 180—
ReactantDiethyl 2-pent-4-enylpropanedioateHCID 361718—
ReactantSodium BicarbonateHCID 516892—
ReactantAluminium lithium hydrideHCID 21226445—
SolventTetrahydrofuranHCID 8028—
Product1,3-Propanediol, 2-(4-pentenyl)-HCID 1109475184.9%

Reaction Steps

A suspension of 13.8 g of lithium aluminium hydride in 500 ml of tetrahydrofuran was treated dropwise under nitrogen at 0°-5° C. within 1 hour with a solution of 33.2 g of diethyl (4-pentenyl)malonate in 125 ml of tetrahydrofuran. The mixture was stirred overnight at room temperature and then heated to boiling for 3 hours. After cooling there were cautiously added dropwise to the reaction mixture firstly 25 ml of acetone and then 25 ml of saturated sodium hydrogen carbonate solution. The resulting slurry was suction filtered and the residue on the suction filter was washed four times with tetrahydrofuran. Concentration of the filtrate gave 17.8 g of 2-(4-pentenyl)-1,3-propanediol (purity 89%) as a yellow liquid.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04709030
Source datasetuspto-grants-1987_11
ORD IDord-2cfe4bbc3277479d8c5031fa66304d2a
Source noteuspto-grants-1987_11