HuagongsheHuagongshe Chemistry Print Report · For research reference only
O-Xylene → 5-(Tetradecyloxy)thiophene-2-carboxylic acid
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | O-Xylene | HCID 7237 | — |
| Reactant | 1-Tetradecanol | HCID 8209 | — |
| Reactant | Sodium hydride | HCID 24758 | — |
| Reactant | 5-Chloro-2-thiophenecarboxylic acid | HCID 95048 | — |
| Solvent | Acetic Acid | HCID 176 | — |
| Product | 5-(Tetradecyloxy)thiophene-2-carboxylic acid | HCID 12361510 | — |
Reaction Steps
A mixture of 21.4 g (0.100 mole) of 1-tetradecanol, 5.9 g (0.146 mole) of sodium hydride (59.5% in oil) and 300 ml of dried xylene is heated to reflux with stirring for 2 hours then allowed to cool after which 7.5 g (0.046 mole ) of 5-chloro-2-thiophenecarboxylic acid is added. The mixture is refluxed for 64 hours after which the mixture is cooled and poured into a water-ice mixture, acidified with acetic acid, and extracted with the addition of ether. The ether is evaporated and aqueous layer extracted 5 times with water: strong ammonia solution (1:1). The combined aqueous extract is acidified with acetic acid. The solid obtained is crystallized twice from hexane to give 5-(tetradecyloxy)-2-thiophene carboxylic acid, M.P. 95°-96° C.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04017514 |
| Source dataset | uspto-grants-1977_04 |
| ORD ID | ord-35b53c1d5a064f24bc7842694e840fd4 |
| Source note | uspto-grants-1977_04 |