Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1363254Generated: October 26, 2026

4-(2-Phenyleth-1-ynyl)thiophene-2-carbaldehyde → 5-Phenethyl-thiophene-2-carbaldehyde

https://huagongshe.com/reaction/1363254

Reaction equation

Participants

RoleNameHCIDCharge
Reactant4-(2-Phenyleth-1-ynyl)thiophene-2-carbaldehydeHCID 2737139—
Reactant5-(Phenylethynyl)thiophene-2-carbaldehydeHCID 2737140—
Reactant4-Phenethylthiophene-2-carbaldehydeHCID 23587414—
Product5-Phenethyl-thiophene-2-carbaldehydeHCID 23587423—

Reaction Steps

5-Phenethylthiophene-2-carbaldehyde was synthesized from 5-(phenylethynyl)thiophene-2-carbaldehyde (4.0 g, 18.8 mmol) following the conditions used to hydrogenate 4-(phenylethynyl)thiophene-2-carbaldehyde to 4-phenethylthiophene-2-carbaldehyde (Example 1.1.b). 5-Phenethylthiophene-2-carbaldehyde (3.8 g, 93%) was used in the next step without further purification 1H NMR (400 MHz, CDCl3) δ (ppm): 9.83 (s, 1H), 7.60 (d, 1H), 7.30 (m, 2H), 7.23 (m, 1H), 7.19 (m, 2H), 6.86 (dt, 1H), 3.21 (t, 2H), 3.03 (t, 2H).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07884124B2
Source datasetuspto-grants-2011_02
ORD IDord-bd4502f16fb046418aed3830ac052056
Source noteuspto-grants-2011_02