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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1646988Generated: November 2, 2026

Hydrochloric Acid → Methyl 6-fluoro-1,2,3,4-tetrahydro-1-oxo-2-naphthalenecarboxylate

https://huagongshe.com/reaction/1646988

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydrochloric AcidHCID 313—
ReactantDimethyl CarbonateHCID 12021—
ReactantSodium hydrideHCID 24758—
Reactant6-Fluoro-1,2,3,4-tetrahydronaphthalen-1-oneHCID 14915116—
SolventDiethyl EtherHCID 3283—
SolventTetrahydrofuranHCID 8028—
SolventHexaneHCID 8058—
ProductMethyl 6-fluoro-1,2,3,4-tetrahydro-1-oxo-2-naphthalenecarboxylateHCID 1992755098.2%

Reaction Steps

Hexane washed sodium hydride (3.5 g of 60%, 88 mmole) was covered with 75 ml of tetrahydrofuran and 5.4 ml (64 mmole) of dimethylcarbonate was added in one portion. The solution was heated to reflux and 6-fluoro-3,4-dihydro-1(2H)-naphthlenone (7.2 g, 44 mmole) in 25 ml of tetrahydrofuran was added dropwise while maintaining reflux. After the addition was complete, the reaction was refluxed for 1.5 hours. The reaction was then cooled in an ice bath and 10% aqueous HCl solution was carefully added. The solution was diluted with ether and the aqueous Phase was separated and extracted twice with ether. The combined organic phases were dried (MgSO4) and concentrated. The crude product was a pale yellow solid (9.6 g, 98% yield).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05182303
Source datasetuspto-grants-1993_01
ORD IDord-21fd0d1133a14d629a2896c883e1a4e3
Source noteuspto-grants-1993_01