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
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Boron trifluoride | HCID 6356 | — |
| Reactant | Myristic Acid | HCID 11005 | — |
| Reactant | 2,3-Dimethylhydroquinone | HCID 69100 | — |
| Reactant | Sodium Acetate | HCID 517045 | — |
| Solvent | Benzene | HCID 241 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | 2,3-Dimethyl-6-myristoyl-hydroquinone | HCID 20510467 | — |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|
| Patent number | US04232107 |
|---|
| Source dataset | uspto-grants-1980_11 |
|---|
| ORD ID | ord-07d8b452c2364852bfe5eaac08c6343c |
|---|
| Source note | uspto-grants-1980_11 |
|---|