Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1731730Generated: November 1, 2026

Trimethyl orthoformate → HCID 13746853, compound

https://huagongshe.com/reaction/1731730

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTrimethyl orthoformateHCID 9005—
Reactant1-DecyneHCID 12997—
ReactantHCID 178418443HCID 178418443—
SolventDiethyl EtherHCID 3283—
ProductHCID 13746853HCID 13746853—

Reaction Steps

To freshly prepared ethyl magnesium bromide (from 61 mmoles bromoethane and 63 mmoles magnesium) was added 1-decyne (50 mmoles) in diethyl ether (10 ml) dropwise at ambient temperature. The reaction mixture was then heated at reflux for 2 hours. After cooling the reaction mixture, trimethylorthoformate (75 mmoles) in diethyl ether (10 ml) was added and the resultant mixture heated to distill off the diethyl ether. The resultant paste was taken up in anhydrous toluene (50 ml) and heated at reflux for 1 hour. The reaction mixture was poured into saturated ammonium chloride (50 ml) and then extracted with diethyl ether (3×50 ml). The organic phase was washed with water (3×20 ml) and dried over anhydrous magnesium sulfate. Evaporation of the organic phase afforded the desired product as an oil.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04623535
Source datasetuspto-grants-1986_11
ORD IDord-9aa4a599ffac4524bd714a62afd62fbd
Source noteuspto-grants-1986_11