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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 704134Generated: October 30, 2026

Potassium Hydroxide → 3,3-Di-(hydroxymethyl)-hexan-1-ol

https://huagongshe.com/reaction/704134

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPotassium HydroxideHCID 14797—
ReactantPotassium Phosphate, DibasicHCID 24450—
ReactantMonobasic potassium phosphateHCID 516951—
ReactantDiethyl 2-prop-1-yl-2-ethoxycarbonylsuccinateHCID 20075591—
ReactantAluminium lithium hydrideHCID 21226445—
SolventAcetic AcidHCID 176—
SolventWaterHCID 962—
SolventDiethyl EtherHCID 3283—
Product3,3-Di-(hydroxymethyl)-hexan-1-olHCID 21885159—

Reaction Steps

Diethyl 2-ethoxycarbonyl-2-n-propyl-succinate (55.8 g) in dry ether (50 ml.) was added slowly to a stirred suspension of lithium aluminium hydride (14.7 g.) in dry ether (150 ml.) at 0°, under a current of nitrogen. The mixture was stirred at room temperature for three hours and then refluxed, with stirring for four hours. A solution of potassium hydroxide (30.0 g.), potassium dihydrogen phosphate (22.0 g.) and potassium monohydrogen phosphate (22.0 g.) in water (200 ml.) was added to the cooled reaction mixture. The pH was adjusted to 5.0 with glacial acetic acid. The solid was removed by filtration and washed with water (40 ml.) The combined filtrates and washings were evaporated in vacuo. The residue was washed with acetone (3×100 ml). The acetone washings were evaporated in vacuo. The residue was washed with chloroform (3×100 ml.) and the washings were evaporated in vacuo, Toluene was added and the residue was evaporated in vacuo. 3,3-Di-(hydroxymethyl)-hexan-1-ol was obtained as a colourless oil and was used without further purification.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04985582
Source datasetuspto-grants-1991_01
ORD IDord-45034e951f444a7ca2b9ba47e95e7606
Source noteuspto-grants-1991_01