HuagongsheHuagongshe Chemistry Print Report · For research reference only
4-(2-Phenyleth-1-ynyl)thiophene-2-carbaldehyde → 5-Phenethyl-thiophene-2-carbaldehyde
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | 4-(2-Phenyleth-1-ynyl)thiophene-2-carbaldehyde | HCID 2737139 | — |
| Reactant | 5-(Phenylethynyl)thiophene-2-carbaldehyde | HCID 2737140 | — |
| Reactant | 4-Phenethylthiophene-2-carbaldehyde | HCID 23587414 | — |
| Product | 5-Phenethyl-thiophene-2-carbaldehyde | HCID 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
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US07884124B2 |
| Source dataset | uspto-grants-2011_02 |
| ORD ID | ord-bd4502f16fb046418aed3830ac052056 |
| Source note | uspto-grants-2011_02 |