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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1911456Generated: October 26, 2026

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

https://huagongshe.com/reaction/1911456

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 numberUS08604022B2
Source datasetuspto-grants-2013_12
ORD IDord-508423769de54726aa99bfca1fb05764
Source noteuspto-grants-2013_12