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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 326290Generated: October 29, 2026

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

https://huagongshe.com/reaction/326290

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 numberUS05268388
Source datasetuspto-grants-1993_12
ORD IDord-0c5802f496d94262be346f01a287f95a
Source noteuspto-grants-1993_12