HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 328374Generated: October 30, 2026
Phosphorus oxychloride → 5-(Hexadecyloxy)thiophene-2-carbaldehyde
https://huagongshe.com/reaction/328374
Participants
| Role | Name | HCID | Charge |
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| Reactant | Phosphorus oxychloride | HCID 24813 | — |
| Reactant | N-Methylformanilide | HCID 66737 | — |
| Reactant | 2-(Hexadecyloxy)thiophene | HCID 21441827 | — |
| Product | 5-(Hexadecyloxy)thiophene-2-carbaldehyde | HCID 21441823 | — |
Reaction Steps
To a cooled mixture of 27 g of N-methylformanilide and 27 g (0.176 mole) of phosphorus oxychloride is added 32.5 g (0.1 mole) of 2-hexadecyloxythiophene. The mixture is warmed to 70° C under vacuum (10 mm Hg). The mixture is allowed to stand at 60°-70° C for 7 hours, the overnight at room temperature after which the mixture is stirred into 100 g of ice. The mixture is extracted into benzene, washed with water, dried over sodium sulfate and distilled in vacuo to give 5-hexadecyloxy-2-thiophenecarboxaldehyde. The carboxaldehyde (7.1 g, 0.02 mole) is stirred vigorously with 4 g of potassium hydroxide in 2.6 ml of water for 24 hours. The mixture is diluted with water and extracted into ether. The aqueous layer is separated and acidified with hydrochloric acid precipitating 5-(hexadecyloxy)-2-thiophenecarboxylic acid.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US04017514 |
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| Source dataset | uspto-grants-1977_04 |
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| ORD ID | ord-cbc5e6d38f4f49a584d12ad8cf9b2c3f |
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| Source note | uspto-grants-1977_04 |
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