HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1415248Generated: November 1, 2026
Trimethylhydroquinone → HCID 21581684, compound
https://huagongshe.com/reaction/1415248
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Trimethylhydroquinone | HCID 12785 | — |
| Reactant | Aluminum(III) Chloride | HCID 6451240 | — |
| Reactant | HCID 15687733 | HCID 15687733 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Solvent | Nitromethane | HCID 6375 | — |
| Product | HCID 21581684 | HCID 21581684 | — |
Reaction Steps
To an ice-cooled mixture of 3.37 g. of aluminum chloride and 40 ml. of methylene chloride was added, dropwise, 3.37 ml. of nitromethane. The resulting solution was stirred 5 minutes, and then 5.114 g. of trimethylhydroquinone was added in one portion. The green mixture was cooled to -20° and a solution of 5.35 g. of 3-hydroxy-3-methyl-4-pentenyl acetate in 20 ml. of methylene chloride was added over 1.0 hour. The mixture was allowed to warm to room temperature, kept there for 2 hours and poured into ice-H2O. The mixture was extracted with methylene chloride and the organic solutions were washed with saturated sodium bicarbonate solution and brine and dried over sodium sulfate. Solvent removal gave crude (±)-2-(2-acetoxyethyl)-6-hydroxy-2,5,7,8-tetramethylchroman as a red oil.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US04003919 |
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| Source dataset | uspto-grants-1977_01 |
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| ORD ID | ord-ee03c0374c04420d9117fbc157e6828a |
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| Source note | uspto-grants-1977_01 |
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