HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1005178Generated: October 29, 2026
Triethylamine → 2-Chloromethyl-4,8-dimethoxy-naphthalene
https://huagongshe.com/reaction/1005178
Participants
| Role | Name | HCID | Charge |
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| Reactant | Triethylamine | HCID 8471 | — |
| Reactant | Methanesulfonyl chloride | HCID 31297 | — |
| Reactant | HCID 22126362 | HCID 22126362 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | 2-Chloromethyl-4,8-dimethoxy-naphthalene | HCID 22126964 | 88.9% |
Reaction Steps
A solution of 3.92 g of methanesulphonyl chloride in 20 ml of methylene chloride was added dropwise to a solution, cooled to -10° C., of 7.7 g (35.3 mmol) of (4,8-dimethoxy-naphthalen-2-yl)-methanol and 4.4 g (38.8 mmol) of triethylamine in 50 ml of methylene chloride. The reaction mixture was stirred at room temperature for 18 hours. For the working-up, the mixture was extracted with 50 ml of ice-cold sodium hydrogen carbonate solution and the aqueous phase was separated and back-extracted with 25 ml of methylene chloride. The combined organic phases were dried over sodium sulphate and subsequently evaporated under reduced pressure. For purification, the residue was filtered over a layer of silica gel using methylene chloride as the eluent. There were obtained 7.2 g of 2-chloromethyl-4,8-dimethoxy-naphthalene as a beige solid; MS: 296 (M)+.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US06051712 |
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| Source dataset | uspto-grants-2000_04 |
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| ORD ID | ord-0733f6ec73fa4a64a508edd503eaf5e3 |
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| Source note | uspto-grants-2000_04 |
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