HuagongsheHuagongshe Chemistry Print Report · For research reference only
Trimethylhydroquinone → HCID 13633545, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Trimethylhydroquinone | HCID 12785 | — |
| Reactant | Ammonium Chloride | HCID 25517 | — |
| Reactant | HCID 54100633 | HCID 54100633 | — |
| Solvent | 1,4-Dioxane | HCID 31275 | — |
| Product | HCID 13633545 | HCID 13633545 | 43.5% |
Reaction Steps
Fused zinc chloride (0.22 g), trimethylhydroquinone (2.47 g) and anhydrous dioxane (10 cc) are introduced into a 250 cc reactor. The mixture is heated to 40°-45° C. and a solution of 1,7,11,15-tetrachloro-3,7,11,15-tetramethylhexadec-2-ene (6.8 g) in dioxane (7 cc) is then added over the course of 20 minutes. Stirring is continued for 1 hour 30 minutes. This reaction mixture is poured into an aqueous solution (50 cc) of ammonium chloride (100 g/liter). The mixture is extracted with ethyl acetate (twice 50 cc) and the organic phases are then dried over magnesium sulphate. After filtration and evaporation of the solvent, 2,5,7,8-tetramethyl-2-(4',8',12'-trichloro-4',8',12'-trimethyltridecyl)-chroman-6-ol is obtained in a yield of 43.5%.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04665244 |
| Source dataset | uspto-grants-1987_05 |
| ORD ID | ord-c30644bfcb2f4484be25561ee7f427c2 |
| Source note | uspto-grants-1987_05 |