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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1462836Generated: October 31, 2026

Methanol → 65416-26-4

https://huagongshe.com/reaction/1462836

Reaction equation

Participants

RoleNameHCIDCharge
ReactantMethanolHCID 887—
ReactantEthyl BromideHCID 6332—
ReactantSodium hydrideHCID 24758—
Reactant(3E)-4-(2,6,6-Trimethyl-1-cyclohexen-1-yl)-3-buten-2-olHCID 5373729—
SolventBenzeneHCID 241—
SolventWaterHCID 962—
Product65416-26-4HCID 643699381.4%

Reaction Conditions

Temperature20 °C

Reaction Steps

A solution of 350 g (1.8 mol) of β-ionol in 600 ml of benzene was allowed to flow in over a period of 15 minutes to a suspension of 97.5 g (2.34 mol) of sodium hydride (ca 55%-60%) in 3 liters of benzene and the mixture was subsequently stirred at reflux for 8 hours. The mixture was cooled to ca 50° C. and treated over a period of 10 minutes with 232 g (2.13 mol) of ethyl bromide. The mixture was stirred at reflux for 20 hours, cooled to 20° C., cautiously treated with 50 ml of methanol and, after 20 minutes, with 1.2 liters of water. The phases were separated, the organic phase was washed with water until neutral, dried and concentrated. Crude distillation of the crude product gave 326 g of crude ether 2 of boiling point 120°-128° C./10 mmHg. Fine distillation finally gave 274 g (68.3%) of pure and olfactorily good β-ionyl ethyl ether 2 of boiling point 121° C./10 mmHg; nD20 =1.4752.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04461309
Source datasetuspto-grants-1984_07
ORD IDord-c4ce314ef6814d89837c2497d4b7828b
Source noteuspto-grants-1984_07