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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2369772Generated: October 30, 2026

Sodium Sulfate → HCID 57429404, compound

https://huagongshe.com/reaction/2369772

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSodium SulfateHCID 24436—
ReactantAluminium lithium hydrideHCID 21226445—
Reactant3-(3-Methylcyclohexyl)propanoic acidHCID 57429405—
SolventDiethyl EtherHCID 3283—
ProductHCID 57429404HCID 5742940464%

Reaction Conditions

Temperature0 °C

Reaction Steps

LiAlH4 (16 g, 0.42 mol, 1.2 eq) and diethyl ether (450 mL) were charged into a 2 L three-necked round-bottom flask equipped with a mechanical stirrer and a reflux condenser and cooled at 0° C. The crude 3-(3-methylcyclohexyl)propanoic acid (60 g, 0.35 mol) was dissolved in diethyl ether (400 mL) and added dropwise to the reaction flask. The reaction mixture was then stirred for 3 h at ambient temperature. The excess of lithium aluminium hydride was hydrolyzed with saturated aqueous sodium sulphate and the mixture filtered. THF (1 L) was added to the residue and the suspension was heated to 35° C. for 1 h. The suspension was filtered and the combined organic layers were dried over sodium sulphate and evaporated to yield the crude product as an oil. Chromatography on a silica gel column with 8% EtOAc in hexane as elution agent, followed by a bulb-to-bulb distillation (0.1 mBar, 140° C.) gave pure 3-(3-methylcyclohexyl)propan-1-ol (35 g, gc purity>98%; yield=61%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08709994B2
Source datasetuspto-grants-2014_04
ORD IDord-d3a0fae7648f4f2b968bbcd0eb9bed62
Source noteuspto-grants-2014_04