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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 16883Generated: October 29, 2026

Allyl bromide → Ethyl 4-(4-allyl-1,4-diazepan-1-yl)benzoate

https://huagongshe.com/reaction/16883

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAllyl bromideHCID 7841—
ReactantDiisopropylethylamineHCID 81531—
ReactantEthyl 4-(1,4-diazepan-1-yl)benzoateHCID 18425301—
SolventDichloromethaneHCID 6344—
ProductEthyl 4-(4-allyl-1,4-diazepan-1-yl)benzoateHCID 6658994748.5%

Reaction Steps

3-Bromoprop-1-ene (0.433 mL, 5.00 mmol) was added to a stirred solution of ethyl 4-(1,4-diazepan-1-yl)benzoate (1.242 g, 5 mmol) and DIPEA (2.183 mL, 12.50 mmol) in dichloromethane (20 mL). The reaction mixture was stirred under nitrogen at room temperature for 24 h. This was diluted with dichloromethane (20 mL), washed with water (2×25 ml) and saturated sodium chloride solution (20 ml), dried over MgSO4, filtered and evaporated to dryness. The crude product was purified by silica column chromatography, eluting with a gradient of 0 to 5% 2.5M ammonia/MeOH in DCM. Pure fractions were evaporated to dryness to afford ethyl 4-(4-allyl-1,4-diazepan-1-yl)benzoate (0.700 g, 48.5%) as a yellow oil.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07737149B2
Source datasetuspto-grants-2010_06
ORD IDord-0f57d7a3fd0848948bd38eb84eb9f07f
Source noteuspto-grants-2010_06