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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2248288Generated: October 27, 2026

Allyl bromide → Methyl 2,3-dihydro-6-fluoro-4-(2-propenyl)-4H-1-benzopyran-4-carboxylate

https://huagongshe.com/reaction/2248288

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAllyl bromideHCID 7841—
ReactantSodium hydrideHCID 24758—
ReactantAmmonium ChlorideHCID 25517—
ReactantMethyl 6-fluorochromane-4-carboxylateHCID 14986536—
SolventDimethylformamideHCID 6228—
ProductMethyl 2,3-dihydro-6-fluoro-4-(2-propenyl)-4H-1-benzopyran-4-carboxylateHCID 19094435—

Reaction Conditions

Temperature0 °C

Reaction Steps

A solution of methyl 6-fluorochromane-4-carboxylate (2.1 g) in anhydrous N,N-dimethylformamide was added to a suspension of sodium hydride (265 mg) in anhydrous N,N-dimethylformamide under nitrogen. After gas evolution ceased, the mixture was cooled to 0° C., and neat allyl bromide (0.95 mL) was added. After 1 hour, 20 mL of an aqueous saturated ammonium chloride solution was added, and the mixture extracted with ethyl acetate, the extracts washed with water, brine, dried over anhydrous sodium sulfate, filtered and evaporated to afford the title compound as a colorless oil, 2.4 g. (HRMS calc'd 250.1004; found 250.1002).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05039672
Source datasetuspto-grants-1991_08
ORD IDord-1e8e33b6c94b4215bb212e3439e4d1e7
Source noteuspto-grants-1991_08