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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 898458Generated: October 30, 2026

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

https://huagongshe.com/reaction/898458

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 numberUS07351728B2
Source datasetuspto-grants-2008_04
ORD IDord-dd18b56d31a045fd98dbd5d441db7e2a
Source noteuspto-grants-2008_04