HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 843412Generated: October 30, 2026
Triethylamine → 3-(Chloromethyl)-1-methoxynaphthalene
https://huagongshe.com/reaction/843412
Participants
| Role | Name | HCID | Charge |
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| Reactant | Triethylamine | HCID 8471 | — |
| Reactant | Methanesulfonyl chloride | HCID 31297 | — |
| Reactant | (4-Methoxynaphthalen-2-yl)methanol | HCID 18755436 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | 3-(Chloromethyl)-1-methoxynaphthalene | HCID 18755443 | — |
Reaction Steps
15.0 g (79.7 mmol) of (4-methoxy-naphthalen-2-yl)-methanol [Chem. Pharm. Bull. 19(6), 1245-1256 (1971)] were dissolved in 100 ml of dichloromethane, the solution treated with 20 ml of triethylamine, cooled to −5° C. and treated slowly with 9.3 ml (119.5 mmol) methanesulfonyl chloride. Then, the reaction mixture was stirred at room temperature for 23 hours, concentrated in a water-jet vacuum, redissolved in 80 ml of tetrahydrofuran, treated with 11.25 g of sodium hydrogen carbonate and stirred for another 2 hours. The suspension was then diluted with 500 ml of water and extracted three times with 300 ml of ethyl acetate, the organic phases were washed once with distilled water, then dried over magnesium sulphate, filtered and concentrated in a water-jet vacuum. The thus-obtained crude product was chromatographed on silica gel with pentane/dichloromethane (4/1). There were thus obtained 11.9 g (57.5 mmol), 72.5% 3-chloromethyl-1-methoxy-naphthalene as a colorless solid; MS: 206 (M)+.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US06376672B1 |
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| Source dataset | uspto-grants-2002_04 |
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| ORD ID | ord-e97b10cb51104a8baae1b0e1d42d3f93 |
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| Source note | uspto-grants-2002_04 |
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