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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 972171Generated: November 1, 2026

Water → 3-Methyl-5-(2,2,3-trimethylcyclopent-3-en-1-yl)pentan-2-ol

https://huagongshe.com/reaction/972171

Reaction equation

Participants

RoleNameHCIDCharge
ReactantWaterHCID 962—
ReactantSodium SulfateHCID 24436—
Reactant3-Cyclopentene-1-butanal, .alpha.,2,2,3-tetramethyl-HCID 6455034—
ReactantHCID 178418348HCID 178418348—
SolventDiethyl EtherHCID 3283—
Product3-Methyl-5-(2,2,3-trimethylcyclopent-3-en-1-yl)pentan-2-olHCID 10321281%

Reaction Conditions

Temperature0 °C

Reaction Steps

A solution of 20.8 g (0.12 mole) of 2-methyl-4-(2,2,3-trimethylcyclopent-3-en-1-yl)butanal dissolved in ethyl ether-anhydrous (50 ml) was added to a stirred solution of methyllithium (1.7 M) in ethyl ether (250 ml; 0.14 mole) which was previously cooled to 0° C. The mixture was stirred at 0°-5° C for 1.0 hour and then heated at reflux (36° C) for 3.0 hours. The mixture was cooled to 0° C and excess methyllithium was decomposed by slow dropwise addition of saturated sodium sulfate solution (50 ml). The mixture was poured into 150 ml of water, the lower aqueous layer was drawn off and extracted twice with 100 ml of ether. The ether extracts were combined, washed with 150 ml of brine, dried over sodium sulfate, filtered and the solvent removed by distillation. The residual oil was fractionally distilled to yield 3-methyl-5-(2,2,3-trimethylcyclopent-3-en-1-yl)pentan-2-ol: 20.4 g (81% yield); bp 96°-98° (0.9 mm); mol wt. 210 (ms).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04052341
Source datasetuspto-grants-1977_10
ORD IDord-41ec6360ae844523abedc380ed177094
Source noteuspto-grants-1977_10