HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1163971Generated: October 25, 2026
Methane, dichloromethoxy- → 7-Fluoronaphthalene-1-carbaldehyde
https://huagongshe.com/reaction/1163971
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Methane, dichloromethoxy- | HCID 21004 | — |
| Reactant | 2-Fluoronaphthalene | HCID 67583 | — |
| Catalyst | Titanium Tetrachloride | HCID 24193 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | 7-Fluoronaphthalene-1-carbaldehyde | HCID 13093562 | 21.1% |
Reaction Steps
By the method of Preparation 1, 2-fluoronaphthalene (10 g., 0.068 mole) in 200 ml. of methylene chloride was reacted with titanium tetrachloride (25.5 g., 14.7 ml. 0.136 mole) and 1,1-dichloromethyl methyl ether (10.1 g., 0.088 mole). The resulting crude product (11 g.) was first recrystallized from hexane to yield 7-fluoro-1-naphthaldehyde [2.5 g., m.p. 95°-96° C., Rf 0.25 (1:1 chloroform:hexane)]. The mother liquor was evaporated to dryness and the residue chromatographed on 400 g. of silica gel, eluting initially with 3:1 hexane:chloroform and then with 3:2 hexane:chloroform. The column was monitored by tlc. Fractions contain clean 2-fluoro-1-naphthaldehyde [Rf 0.31 (3:2 hexane:chloroform)] were combined and evaporated to dryness, yielding purified 2-fluoro-1-naphthaldehyde (2.8 g., m.p. 60°-62° C.).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US04367234 |
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| Source dataset | uspto-grants-1983_01 |
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| ORD ID | ord-2d69065330ac4f52bb9ea8e8dd852c32 |
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| Source note | uspto-grants-1983_01 |
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