HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1030430Generated: November 1, 2026
Dimethylformamide → 6-Ethoxy-2,5,7,8-tetramethyl-2-(4-nitrophenoxymethyl)chroman
https://huagongshe.com/reaction/1030430
Participants
| Role | Name | HCID | Charge |
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| Reactant | Dimethylformamide | HCID 6228 | — |
| Reactant | Iodoethane | HCID 6340 | — |
| Reactant | Sodium hydride | HCID 24758 | — |
| Reactant | 6-Hydroxy-2,5,7,8-tetramethyl-2-(4-nitrophenoxymethyl)chroman | HCID 13488869 | — |
| Solvent | Benzene | HCID 241 | — |
| Solvent | Water | HCID 962 | — |
| Product | 6-Ethoxy-2,5,7,8-tetramethyl-2-(4-nitrophenoxymethyl)chroman | HCID 19822195 | — |
Reaction Steps
1.6 g of a 55% w/w suspension of sodium hydride in mineral oil was added to a mixture of 11 g of 6-hydroxy-2,5,7,8-tetramethyl-2-(4-nitrophenoxymethyl)chroman and 100 ml of dimethylformamide, and the reaction mixture was stirred for 1 hour at room temperature. Then a mixture of 5.7 g of ethyl iodide and 5 ml of benzene was added dropwise, whilst ice-cooling, and the reaction mixture was stirred for 2 hours at room temperature. The reaction mixture was then poured into water and extracted with benzene. This extract was washed with water and dried over anhydrous sodium sulfate. The solvent was distilled from the extract under reduced pressure, and the residue was purified by silica gel column chromatography eluted with a 3:7 by volume mixture of cyclohexane and benzene, to give the title compound.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US05104888 |
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| Source dataset | uspto-grants-1992_04 |
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| ORD ID | ord-d9c72a3d8deb4c689e8213fe6637da30 |
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| Source note | uspto-grants-1992_04 |
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