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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2208759Generated: November 1, 2026

Allyl bromide → HCID 86719546, compound

https://huagongshe.com/reaction/2208759

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAllyl bromideHCID 7841—
ReactantSodium hydrideHCID 24758—
ReactantHCID 70873719HCID 70873719—
SolventDimethylformamideHCID 6228—
ProductHCID 86719546HCID 8671954629.4%

Reaction Conditions

Temperature0 °C

Reaction Steps

Methyl 5-chloro-3-(cyclopentylamino)-2-methylbenzoate (1.2 g, 4.46 mmol) was dissolved in DMF (12 mL) and cooled to 0° C. NaH (0.21 g, 8.92 mmol) was added after 10 minutes and allyl bromide (1.07 g, 8.9 mmol) was added. The reaction mixture was stirred at room temperature for 4 h and then heated at 80 0° C. for 18 h. The reaction was quenched with ice water and extracted with ethyl acetate. Combined organic layers were dried, concentrated giving crude methyl 3-(allyl(cyclopentyl)amino)-5-chloro-2-methylbenzoate (0.4 g, 29.4%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09376422B2
Source datasetuspto-grants-2016_06
ORD IDord-f12829de176c4fb0818212140342c2df
Source noteuspto-grants-2016_06