Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 224467Generated: October 25, 2026

Boron trifluoride → 2,3-Dimethyl-6-myristoyl-hydroquinone

https://huagongshe.com/reaction/224467

Reaction equation

Participants

RoleNameHCIDCharge
ReactantBoron trifluorideHCID 6356—
ReactantMyristic AcidHCID 11005—
Reactant2,3-DimethylhydroquinoneHCID 69100—
ReactantSodium AcetateHCID 517045—
SolventBenzeneHCID 241—
SolventDichloromethaneHCID 6344—
Product2,3-Dimethyl-6-myristoyl-hydroquinoneHCID 20510467—

Reaction Conditions

Temperature50 °C

Reaction Steps

Boron trifluoride was introduced with vigorous refluxing (bath temperature 50° C.) into a mixture of 138 g (1 mole) of 2,3-dimethylhydroquinone, 370 g (1.62 moles) of myristic acid and 700 ml of methylene chloride until saturation. After standing overnight the reaction mixture was decomposed by pouring into 3 l of a 10% by weight sodium acetate solution with stirring. The methylene chloride was evaporated by means of steam. The residual oily layer solidified after cooling to a melt cake that was isolated by decantation. It was melted up and added with stirring to 2 l of high-boiling benzine. The precipitate was filtered with suction and washed with benzine (boiling range: 50°-75° C.). After being dried the precipitate was stirred with acetonitrile and filtered with suction.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04232107
Source datasetuspto-grants-1980_11
ORD IDord-07d8b452c2364852bfe5eaac08c6343c
Source noteuspto-grants-1980_11