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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 253297Generated: October 30, 2026

Water → (7-Fluoro-2,3-dihydro-1,4-benzodioxine-5-yl)methanol

https://huagongshe.com/reaction/253297

Reaction equation

Participants

RoleNameHCIDCharge
ReactantWaterHCID 962—
ReactantSodium HydroxideHCID 14798—
ReactantAluminium lithium hydrideHCID 21226445—
ReactantMethyl 7-fluoro-2,3-dihydro-1,4-benzodioxine-5-carboxylateHCID 49780160—
SolventTetrahydrofuranHCID 8028—
Product(7-Fluoro-2,3-dihydro-1,4-benzodioxine-5-yl)methanolHCID 66891450100%

Reaction Steps

A solution of methyl 7-fluoro-2,3-dihydro-1,4-benzodioxine-5-carboxylate (400 mg, 1.88 mmol) in tetrahydrofuran (20 mL) was cooled to 0° C. and then added lithium aluminum hydride (3.78 mL, 1.0 M solution in tetrahydrofuran). The reaction mixture was allowed to warm to room temperature and stirred for 45 min, at which time water (143 μL) was added followed by 15% sodium hydroxide (143 μL) and then water (286 μL) again. The white precipitate was filtered and the filtrate was concentrated to give 345 mg (100%) of (7-fluoro-2,3-dihydro-1,4-benzodioxine-5-yl)methanol as a colorless oil: 1H NMR (400 MHz, CDCl3): 6.63 (dd, J=2.8, 8.8 Hz, 1H), 6.56 (dd, J=3.2, 9.2 Hz, 1H), 4.64 (d, J=6.4 Hz, 2H), 4.28-4.25 (m, 4H).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07872014B2
Source datasetuspto-grants-2011_01
ORD IDord-bcc5e22d09ea44309364b0e3c64cfd25
Source noteuspto-grants-2011_01