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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1906880Generated: November 1, 2026

Benzene → 6-Fluoro-3,4-dihydro-2H-1-benzopyran-2-methanol

https://huagongshe.com/reaction/1906880

Reaction equation

Participants

RoleNameHCIDCharge
ReactantBenzeneHCID 241—
ReactantHydrochloric AcidHCID 313—
ReactantEthanolHCID 702—
Reactant2H-1-Benzopyran-2-carboxylic acid, 6-fluoro-3,4-dihydro-, ethyl esterHCID 21936879—
SolventWaterHCID 962—
SolventTolueneHCID 1140—
SolventDiethyl EtherHCID 3283—
Product6-Fluoro-3,4-dihydro-2H-1-benzopyran-2-methanolHCID 1178864585%

Reaction Conditions

Temperature15 °C

Reaction Steps

To a stirred mixture of 50 parts of ethyl 6-fluoro-3,4-dihydro-2H-1-benzopyran-2-carboxylate and 540 parts of benzene were added dropwise, during a 1 hour-period, a mixture of 89 parts of a solution of sodium dihydro-bis(2-methoxyethoxy)aluminate in methylbenzene (3.4M) and 135 parts of benzene at reflux temperature and under nitrogen atmosphere. Upon completion, stirring was continued for 2.5 hours at reflux. After cooling to 15° C., the reaction mixture was decomposed by the dropwise addition of 24 parts of ethanol and 10 parts of water. The reaction mixture was poured onto ice water. Concentrate hydrochloric acid and 350 parts of 1,1'-oxybisethane were added. The organic layer was separated, washed with water, dried, filtered and evaporated. The oily residue was purified by column chromatography over silica gel using trichloromethane as eluent. The pure fractions were collected and the eluent was evaporated, yielding 34 parts (85%) of 6-fluoro-3,4-dihydro-2H-1-benzopyran-2-methanol as an oily residue (intermediate 7).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04654362
Source datasetuspto-grants-1987_03
ORD IDord-0bc697c8c2ce439a99271b63d3339b7a
Source noteuspto-grants-1987_03