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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1609956Generated: October 31, 2026

Allyl bromide → 4-(Phenylmethoxy)-2-(2-propen-1-yl)-1-(2-propen-1-yloxy)benzene

https://huagongshe.com/reaction/1609956

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAllyl bromideHCID 7841—
ReactantCesium carbonateHCID 10796—
ReactantHCID 18701949HCID 18701949—
SolventMethyl Ethyl KetoneHCID 6569—
Product4-(Phenylmethoxy)-2-(2-propen-1-yl)-1-(2-propen-1-yloxy)benzeneHCID 22261130—

Reaction Steps

A mixture of 2-allyl-4-benzyloxy-phenol (ER2-YYR-17) (35.56 g, 148 mmol), allyl bromide (21.5 g, 178 mmol), cesium carbonate (58 g, 178 mmol) and methyl ethyl ketone (400 mL) was refluxed with stirring in a 1 L round bottomed flask. After 23 h, the reaction was cooled and concentrated. The residue was partitioned between water (500 mL) and EtOAc (400 mL). The organic layer was dried (MgSO4) and concentrated to a tan oil, 39.37 (95%) ER0-LKW-190A: 1H NMR (CDCl3) δ 3.45 (dd, 2H), 4.54 (dd, 2H), 5.04 (s, 2H), 5.18 (m, 2H), 5.29 (dd, 1H), 5.46 (dd, 1H), 5.94-6.18 (m, 2H), 6.81 (s, 2H), 6.88 (s, 1H), 7.30-7.48 (m, 5H), MS (ES) m/e 281 [M+1].

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06982278B2
Source datasetuspto-grants-2006_01
ORD IDord-f85cdc82b0e242e5b7c4f4c1fc32151f
Source noteuspto-grants-2006_01