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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2218757Generated: October 30, 2026

Ammonium Chloride → 8-Fluoro-10,11-dihydro-5-methylene-5H-benzo[4,5]cyclohepta[1,2-b]pyridine

https://huagongshe.com/reaction/2218757

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAmmonium ChlorideHCID 25517—
Reactant8-Fluoro-10,11-dihydro-5H-benzo[4,5]cyclohepta[1,2-b]pyridin-5-oneHCID 44203204—
ReactantHCID 178418573HCID 178418573—
SolventTetrahydrofuranHCID 8028—
Product8-Fluoro-10,11-dihydro-5-methylene-5H-benzo[4,5]cyclohepta[1,2-b]pyridineHCID 59769972—

Reaction Steps

Chill a mixture of 8-fluoro-10,11-dihydro-benzo[4,5]cyclohepta[1,2-b]pyridin-5-one (1.3 g, 5.7 mmol) and dry tetrahydrofuran (50 mL) to 0° C. Treat this mixture with methyl magnesium bromide(3.0M solution in diethyl ether, 5.7 mL, 17.2 mmol). Remove cooling and stir the admixture at room temperature for 15 min. Quench the reaction, while cooling with an ice-water bath, by adding saturated aqueous ammonium chloride solution (50 mL). Separate the layers and extract the aqueous layer with methylene chloride (2×50 mL). Dry the combined organic layers with magnesium sulfate, filter and concentrate to provide the intermediate product as a thick crude oil.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07411072B2
Source datasetuspto-grants-2008_08
ORD IDord-003e0785793545458001c6d31ffc2406
Source noteuspto-grants-2008_08