HuagongsheHuagongshe Chemistry Print Report · For research reference only
Water → (S)-4-(2,5-dimethoxy-3,4,6-trimethylphenyl)-2-methyl-1,2-butanediol
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Water | HCID 962 | — |
| Reactant | Sodium hydride | HCID 24758 | — |
| Reactant | 1,4-Dimethoxy-2,3,5,6-tetramethylbenzene | HCID 601765 | — |
| Reactant | (2R)-2-methyl-3-chloropropane-1,2-diol | HCID 11469077 | — |
| Solvent | 1,4-Dioxane | HCID 31275 | — |
| Product | (S)-4-(2,5-dimethoxy-3,4,6-trimethylphenyl)-2-methyl-1,2-butanediol | HCID 11129761 | 88.7% |
Reaction Steps
2.4 g (19.6 mmol) of (2R)-2-methyl-3-chloropropane-1,2-diol and 4.28 g (22 mmol) of 2,5-dimethoxy-1,3,4,6-tetramethylbenzene were dissolved in 20 ml of dioxane and heated to reflux temperature within 1 hour with 1.27 g (66 mmol) of sodium hydride (80% in mineral oil) and 0.1 ml of polyethylene glycol 400 (as the phase transfer catalyst) and stirred at this temperature for 16 hours. The mixture was then treated with 50 ml of water, filtered and washed with water. The residue was recrystallized from ether/hexane and there were obtained 4.91 g of (2S)-2-methyl-4-(2,5-dimethoxy-3,4,6-trimethylphenyl)-1,2-butanediol in the form of white crystals with a melting point of 82°-84° C. and [α]D20 =+2.86° (c=1.5% in CHCl3).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04808736 |
| Source dataset | uspto-grants-1989_02 |
| ORD ID | ord-9ff4b8c3172e4fa6a37d7b03ecd59a5b |
| Source note | uspto-grants-1989_02 |