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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2382103Generated: October 31, 2026

Allyl bromide → HCID 68555530, compound

https://huagongshe.com/reaction/2382103

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAllyl bromideHCID 7841—
ReactantCesium carbonateHCID 10796—
ReactantHCID 68557507HCID 68557507—
SolventDimethylformamideHCID 6228—
ProductHCID 68555530HCID 6855553085%

Reaction Steps

A mixture of (3-chloro-pyridin-3-yl)-carbamic acid tert-butyl ester (8.4 g, 36.8 mmol), allyl bromide (7.46 g, 39.1 mmol) and cesium carbonate (24.9 g, 76.4 mmol) in DMF (100 mL) is heated at 600 C. for 1 h. The reaction is quenched with water, extracted with EtOAc. The organic layer is dried (Na2SO4), filtered, and concentrated in vacuo. The residue is purified by silica gel chromatography eluting with 0-40% EtOAc in heptane to afford allyl-(3-chloro-pyridin-3-yl)-carbamic acid tert-butyl ester (8.4 g, 85%). MS: 269 (M+H); 1H NMR (300 MHz, CDCl3): δ=8.66 (s, 1H), 8.49 (d, 1H), 7.18 (d, 1H), 5.80-5.96 (m, 1H) 5.15 (s, 1H), 5.10(d, 1H), 4.2 (broad s, 1H), 1.43 (s, 9H).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08258130B2
Source datasetuspto-grants-2012_09
ORD IDord-b0b58e73a4224154b41981ec4f49bd9d
Source noteuspto-grants-2012_09