HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 247635Generated: October 28, 2026
tert-Butyl hydroperoxide → (2R,3R)-4-(2',5'-dimethoxy-3',4',6'-trimethylphenyl)-2,3-epoxy-2-methylbutanol
https://huagongshe.com/reaction/247635
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | tert-Butyl hydroperoxide | HCID 6410 | — |
| Reactant | Sodium Hydroxide | HCID 14798 | — |
| Reactant | Dibutyl D-tartrate | HCID 6992610 | — |
| Reactant | 4-(2',5'-Dimethoxy-3',4',6'-trimethylphenyl)-2-methyl-2-butenol | HCID 54214616 | — |
| Catalyst | Titanium isopropoxide | HCID 11026 | — |
| Solvent | Diethyl Ether | HCID 3283 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | (2R,3R)-4-(2',5'-dimethoxy-3',4',6'-trimethylphenyl)-2,3-epoxy-2-methylbutanol | HCID 18602181 | 98% |
Reaction Steps
0.594 ml of titanium tetraisopropoxide was dissolved in 10 ml of dry methylene chloride. Thereupon, 524 mg of dibutyl D-tartrate were added dropwise at -20° C. and the mixture was left to stand at -20° C. for 10 minutes. 197 mg of 4-(2',5'-dimethoxy-3',4',6'-trimethylphenyl)-2-methyl-2-butenol were then added and subsequently a further 180 mg of tert.butyl hydroperoxide (80%) were added dropwise (as a solution in 0.5 ml of methylene chloride). The thus-obtained yellow solution was left to stand at -20° C. for 4 to 5 days, then treated with 5 ml of 1N sodium hydroxide solution, left to warm to room temperature and stirred for 1 hour. The phases were then separated, the aqueous phase was washed twice with methylene chloride, the organic phases were dried over sodium sulphate and concentrated. The colourless oil obtained was dissolved in 20 ml of ethyl ether and stirred with 5 ml of 1N sodium hydroxide solution for 1 hour. The phases were again separated, the aqueous phase was washed twice with ethyl ether, the organic phases were dried over sodium sulphate and concentrated. There were obtained 188 mg (98%) of (2R,3R)-4-(2',5'-dimethoxy-3',4',6'-trimethylphenyl)-2,3-epoxy-2-methylbutanol.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US04709055 |
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| Source dataset | uspto-grants-1987_11 |
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| ORD ID | ord-60d80088032f4a68a2aacbc59f880feb |
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| Source note | uspto-grants-1987_11 |
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