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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 628608Generated: October 24, 2026

2-Bromobenzaldehyde → Ethyl 3-(3-formylphenyl)but-2-enoate

https://huagongshe.com/en/reaction/628608

Reaction equation

Participants

RoleNameHCIDCharge
Reactant2-BromobenzaldehydeHCID 81129—
ReactantEthyl trans-crotonateHCID 429065—
ProductEthyl 3-(3-formylphenyl)but-2-enoateHCID 86632145—

Reaction Steps

Coupling of 3 bromobenzaldehyde with ethyl crotonate following the method used in Example 26 gave ethyl 3-(3-formylphenyl)but-2-enoate as a light yellow oil Yield (0.547, 23%): 1H NMR (300 MHz, CDCl3) δ 10.05 (s, 1H), 7.99 (t, J=1.6 Hz, 1H), 7.87 (dt, J=7.6, 1.3 Hz, 1H), 7.74 (m, 1H), 7.56 (t, J=7.6 Hz, 1H), 6.19 (q, J=1.2 Hz, 1H), 4.23 (q, J=7.2 Hz, 2H), 2.61 (d, J=1.2 Hz, 3H), 1.33 (t, J=7.2 Hz, 3H).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09314467B2
Source datasetuspto-grants-2016_04
ORD IDord-8836aa34becb4d87ab276facbf2eace2
Source noteuspto-grants-2016_04