HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 973296Generated: October 29, 2026
Methanol → 2-Chloro-6-chloromethylnaphthalene
https://huagongshe.com/reaction/973296
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Methanol | HCID 887 | — |
| Reactant | Thionyl Chloride | HCID 24386 | — |
| Reactant | (6-Chloronaphthalen-2-yl)methanol | HCID 13384253 | — |
| Solvent | Pyridine | HCID 1049 | — |
| Solvent | Chloroform | HCID 6212 | — |
| Product | 2-Chloro-6-chloromethylnaphthalene | HCID 13384255 | 95.7% |
Reaction Steps
Thionyl chloride (99.4 g.) is added dropwise at 0° C. during 1 hour to a stirred suspension of the 6-chloro-2-hydroxymethylnaphthalene (96.3 g.) in a mixture of pyridine (59.0 g.) and chloroform (2 3 l). The mixture is stirred for 1 hour at 20° C., then treated dropwise with methanol (60 ml.) and stored for 18 hours. The solution is washed with water, 3N-hydrochloric acid, and water again, dried with magnesium sulphate and evaporated. The residue is crystallised from light petroleum (b.p. 80°-100° C.) to give 2-chloromethyl-6-chloronaphthalene (101 g.) m.p. 107°-110° C. raised to 110°-111° C. by further crystallisation.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US04055595 |
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| Source dataset | uspto-grants-1977_10 |
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| ORD ID | ord-b2bad1cb85994e0889e1bf6222282bd6 |
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| Source note | uspto-grants-1977_10 |
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