HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 358176Generated: October 29, 2026
Dimethyl Sulfate → HCID 54497275, compound
https://huagongshe.com/reaction/358176
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Dimethyl Sulfate | HCID 6497 | — |
| Reactant | Hexane | HCID 8058 | — |
| Reactant | 2,4-Dimethyl-2-(2-methylanilino)dioxolane | HCID 54146150 | — |
| Reactant | Butyllithium | HCID 178418339 | — |
| Solvent | Water | HCID 962 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | HCID 54497275 | HCID 54497275 | — |
Reaction Steps
10.0 g (0.048 mole) of 2,4-dimethyl-2-(2-methylanilino)dioxolane was dissolved in about 150 ml of tetrahydrofuran and then cooled to -60° C. 30.15 ml of 1.6 molar n-butyl lithium in hexane (0.048 mole of n-butyl lithium) was added and the temperature of the mixture allowed to raise to 0° C. 4.6 ml (0.048 mole) of dimethyl sulfate was added dropwise at about 0°-10° C. The temperature of the mixture was allowed to raise to 25° C., then refluxed for 3 hours and then stirred overnight (about 15 hours) at room temperature. The mixture was then mixed with about 500 ml of water and extracted with ethyl ether. The ethyl ether extracts were combined, dried over magnesium sulfate and evaporated to dryness affording the title compound as an oil.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US04465502 |
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| Source dataset | uspto-grants-1984_08 |
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| ORD ID | ord-4e9c8b1ba657490884709c303d65372b |
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| Source note | uspto-grants-1984_08 |
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