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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1973977Generated: November 1, 2026

Hydrochloric Acid → HCID 53674838, compound

https://huagongshe.com/reaction/1973977

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydrochloric AcidHCID 313—
ReactantDichloromethaneHCID 6344—
Reactant2-Chloro-N,N-diethyl-1,1,2-trifluoroethan-1-amineHCID 136184—
ReactantHCID 21408131HCID 21408131—
SolventWaterHCID 962—
ProductHCID 53674838HCID 53674838—
ProductHCID 86733917HCID 86733917—

Reaction Steps

A mixture of 25 g. of methyl 6-methoxy-1-hydroxy-1,2,3,4-tetrahydro-2-naphthylacetate, 38 g. of 1-diethylamino-1,1,2-trifluoro-2-chloroethane and 150 ml. of methylene chloride are allowed to stand for 24 hours. The fluorination reaction mixture is added to 250 ml. of water containing 12 g. of hydrogen chloride; the resulting mixture is separated and the methylene chloride phase is washed with water, dried over sodium sulfate, and evaporated to yield methyl 6-methoxy-1-fluoro-1,2,3,4-tetrahyro-2-naphthylacetate and 6-methoxy-1,2-dihydro-2-naphthylacetate. The mixture is separated on alumina eluting with acetone: diethyl ether (1:4) and the separated fractions are identified by ultraviolet spectroscopy. The fraction containing methyl 6-methoxy-1-fluoro-2-naphthylacetate is evaporated and the residue is refluxed with 23 g. of 2,3-dichloro-5,6-dicyano-1,4-benzoquinone and 500 ml. of xylene for six hours. The cooled mixture is filtered and chromatographed on alumina eluting with chloroform. The fraction containing the product is evaporated to yield methyl 6-methoxy-1-fluoro- 2-naphthylacetate.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS03998966
Source datasetuspto-grants-1976_12
ORD IDord-ded4e7778624498c8f68a1b61df95a93
Source noteuspto-grants-1976_12