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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1384321Generated: October 30, 2026

Benzyl Bromide → 6-Fluoro-7-benzyloxychroman-4-one

https://huagongshe.com/reaction/1384321

Reaction equation

Participants

RoleNameHCIDCharge
ReactantBenzyl BromideHCID 7498—
ReactantPotassium CarbonateHCID 11430—
Reactant6-fluoro-7-hydroxy-3,4-dihydro-2H-1-benzopyran-4-oneHCID 21186600—
SolventAcetoneHCID 180—
Product6-Fluoro-7-benzyloxychroman-4-oneHCID 2118659073%

Reaction Steps

A mixture of 6-fluoro-7-hydroxychroman-4-one (the compound of Preparation 29, 0.93 g, 5.11 mmol), benzyl bromide (0.61 mL, 5.13 mmol), potassium carbonate (1.41 g, 10.2 mmol) in acetone (100 mL) was stirred at ambient temperature overnight. The mixture was cooled, filtered, and concentrated to a yellow solid. This residue was recrystallized from ethyl acetate/ether to give 1.02 g (73%) of 6-fluoro-7-benzyloxychroman-4-one in two crops as cream white crystals which had: mp 155-156° C.; NMR δ7.58 (d, J=11 Hz, 1 H), 7.46-7.33 (m, 5 H), 6.54 (d, J=6.7 Hz, 1 H), 5.16 (d, 2 H), 4.50 (t, J=6.4 Hz, 2 H), 2.75 (t, J=6.4 Hz, 2 H). Analysis calculated for C16H13FO2: C, 70.58; H, 4.81. Found: C, 70.45; H, 4.80.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06258827B1
Source datasetuspto-grants-2001_07
ORD IDord-6835b40a682e40d0a3c9b9a1b3ad3184
Source noteuspto-grants-2001_07