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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1363192Generated: October 26, 2026

3,4-Dihydro-2H-1-benzopyran-4-amine → 5-Fluoro-4-Chromanone

https://huagongshe.com/reaction/1363192

Reaction equation

Participants

RoleNameHCIDCharge
Reactant3,4-Dihydro-2H-1-benzopyran-4-amineHCID 4961957—
Reactant6-Methoxychroman-4-amineHCID 12792148—
Reactant8-Fluorochroman-4-amineHCID 16244403—
Reactant6-Chloro-chroman-4-ylamineHCID 16244412—
Reactant6-fluoro-3,4-dihydro-2H-1-benzopyran-4-amineHCID 16244413—
Reactant6-Methylchroman-4-amineHCID 16244417—
Reactant5-Fluorochroman-4-amineHCID 59704898—
Product5-Fluoro-4-ChromanoneHCID 45489795—

Reaction Steps

These amines were prepared via procedures described in Example 29 for the synthesis of 8-fluorochroman-4-amine. The corresponding chroman-4-ones were commercially available as advanced intermediates for the synthesis of chroman-4-amine, 6-fluorochroman-4-amine, 6-chlorochroman-4-amine, 6-methylchroman-4-amine, and 6-methoxychroman-4-amine. For the synthesis of 5-fluorochroman-4-amine, the intermediate 5-fluorochroman-4-one was obtained using procedures from GB 2355264, which also provided 7-fluorochroman-4-one. 7-Fluorochroman-4-one could be used in the synthesis of 7-fluorochroman-4-amine. Chroman-4-amine, 5-fluorochroman-4-amine, 6-fluorochroman-4-amine, 7-fluorochroman-4-amine, 5,8-difluorochroman-4-amine, and 6,8-difluorochroman-4-amine were resolved via the procedure described in Example 29 for the resolution of 8-fluorochroman-4-amine.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07884109B2
Source datasetuspto-grants-2011_02
ORD IDord-694aaad3b098485b86c23cf2a08cc62e
Source noteuspto-grants-2011_02