HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 628229Generated: October 29, 2026
Oxalyl chloride → 5-(2-Hexyldecyl)-2-thiophenecarbonyl chloride
https://huagongshe.com/reaction/628229
Participants
| Role | Name | HCID | Charge |
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| Reactant | Oxalyl chloride | HCID 65578 | — |
| Reactant | HCID 86696620 | HCID 86696620 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | 5-(2-Hexyldecyl)-2-thiophenecarbonyl chloride | HCID 86696619 | 88.4% |
Reaction Steps
5-(2-Hexyldecyl)-2-thiophenecarboxylic acid (1.00 g, 2.84 mmol., 1.00 equiv.) and CH2Cl2 (5 mL) were added to a 10 mL schlenk flask. The solution was cooled to 0° C. Oxalyl chloride (0.60 mL, 6.5 mmol, 2.3 equiv.) was then added. The ice/water bath was left in place and the solution was stirred for 64 hours while warming to room temperature. The reaction mixture was concentrated to a clear brown liquid (931 mg, 88% yield). 1H NMR (400 MHz, CDCl3) δ 7.84 (d, J=3.9 Hz, 1H), 6.87 (d, J=3.8 Hz, 1H), 2.81 (d, J=6.7, 2H), 1.68 (b, 1H), 1.34-1.19 (m, 24H), 0.93-0.85 (m, 6H).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US09312492B2 |
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| Source dataset | uspto-grants-2016_04 |
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| ORD ID | ord-2aef2b0d03974a3f91b2de5a7668cc44 |
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| Source note | uspto-grants-2016_04 |
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