HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1907006Generated: October 30, 2026
Trimethylamine → 1,1-Dimethoxy-1-(6-methoxy-2-naphthyl)prop-2-yl methanesulfonate
https://huagongshe.com/reaction/1907006
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Trimethylamine | HCID 1146 | — |
| Reactant | Methanesulfonyl chloride | HCID 31297 | — |
| Reactant | 1,1-Dimethoxy-1-(6-methoxy-2-naphthyl)propan-2-ol | HCID 11300347 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | 1,1-Dimethoxy-1-(6-methoxy-2-naphthyl)prop-2-yl methanesulfonate | HCID 12756330 | — |
Reaction Steps
The crude oil, 1,1-dimethoxy-1-(6-methoxy-2-naphthyl)propan-2-ol, from Example 5 is dissolved in 250 ml of methylene chloride and cooled to 10° C. Then 12.2 g of trimethylamine is added and the reaction mixture is cooled to about 5° C. Over a 15 minute period, 10.55 g of methanesulfonyl chloride is added. The reaction mixture is stirred for about 30 minutes at 0°-5° C. Separation of the triethylamine hydrochloride as a precipitate is observed. The reaction mixture then is poured into 200 ml of water and extracted with methylene chloride. The organic phase is separated, dried over magnesium sulfate and evaporated under reduced pressure to yield 1,1-dimethoxy-1-(6-methoxy-2-naphthyl)prop-2-yl methanesulfonate as an oil.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US04654438 |
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| Source dataset | uspto-grants-1987_03 |
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| ORD ID | ord-90f530cbead24e158d98b3855819324e |
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| Source note | uspto-grants-1987_03 |
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