HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 840028Generated: October 30, 2026
Hydrochloric Acid → HCID 70589990, compound
https://huagongshe.com/reaction/840028
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Hydrochloric Acid | HCID 313 | — |
| Reactant | Ethanol | HCID 702 | — |
| Reactant | Sodium Hydroxide | HCID 14798 | — |
| Reactant | Methyl 6-methyl-2-naphthyl-alpha-chloroacetate | HCID 86733920 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | HCID 70589990 | HCID 70589990 | — |
Reaction Steps
A mixture of 25 g. of methyl 6-methyl-2naphthyl-α-chloroacetate, 10 g. of sodium hydroxide, and 200 ml. of ethanol is refluxed for 2 hours. The cooled mixture is acidified by the addition of 1N hydrochloric acid. The resulting product, methyl 6-methyl-2naphthyl-α-hydroxyacetate, is isolated by extractions with methylene chloride. The product is oxidized by means of the oxidation procedure described in Example 6 to give methyl 6-methyl-2-naphthyl-α-oxoacetate. The latter product is refluxed with 31 g. of difluoromethylene triphenyl phosphorane (prepared by allowing sodium chlorodifluoroacetate to react with triphenyl phosphine in diethyl ether) in 150 ml. of benzene. The resulting mixture is distilled under vacuum. The distillate is evaporated to yield methyl 2-naphthyl-α,α-difluoromethyleneacetate.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US04097674 |
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| Source dataset | uspto-grants-1978_06 |
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| ORD ID | ord-b8c308fa6b9143e8a45e22450b129c99 |
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| Source note | uspto-grants-1978_06 |
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