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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 444415Generated: October 30, 2026

Hydrochloric Acid → 7-Octen-1-ol, 7-methyl-3-methylene-

https://huagongshe.com/reaction/444415

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydrochloric AcidHCID 313—
ReactantDimethyl SulfideHCID 1068—
ReactantAmmonium ChlorideHCID 25517—
Reactant1-Trimethylsilyloxy-3-butyneHCID 2760858—
ReactantDiethylether pentaneHCID 21877078—
SolventDiethyl EtherHCID 3283—
Product7-Octen-1-ol, 7-methyl-3-methylene-HCID 11435062—

Reaction Steps

2.1 Grams (10.0 mmol) of the above complex is suspended in 15 ml of dry ether, and 12 ml of dimethyl sulfide is added under nitrogen. The resulting solution is cooled to -60° and another 14 ml of dimethyl suflide is added to dissolve the precipitate that forms. The Grignard reagent (24 ml, 9.6 mmol) from B above is added at -60° over 5 min and the reaction is stirred at -45° for 2 hr. Trimethylsilyl 3-butynyl ether (1.4 g, 9.8 mmol) (preparation follows) in ether/pentane (5 ml/30 ml) is added at -45°; the mixture is allowed to warm to -25° with stirring for several hours. The reaction is then poured into a pre-cooled (<-10°) solution of HCl/sat. NH4Cl, allowed to warn to RT and stirred overnight. The reaction is worked up by water and extraction with ether (2×). The ether phases are combined, washed with sat (NH4)2SO4, water and brine, filtered and solvent removed to give 7-methyl-3-methylene-7-octen-1ol.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04264518
Source datasetuspto-grants-1981_04
ORD IDord-f90f07a66ccb40a5a4e12733cb896cd1
Source noteuspto-grants-1981_04