HuagongsheHuagongshe Chemistry Print Report · For research reference only
Triethylamine → 2-Nitrobenzyl perfluorooctanoate
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Triethylamine | HCID 8471 | — |
| Reactant | Triethylamine hydrochloride | HCID 11130 | — |
| Reactant | 2-Nitrobenzyl alcohol | HCID 11923 | — |
| Reactant | Perfluorooctanoyl chloride | HCID 78978 | — |
| Solvent | Benzene | HCID 241 | — |
| Product | 2-Nitrobenzyl perfluorooctanoate | HCID 15095406 | — |
Reaction Steps
Perfluorooctanoyl chloride (21.6 g, 0.05 mol) was added slowly with stirring to a solution of 2-nitrobenzyl alcohol (7.65 g, 0.05 mol) and triethylamine (5.2 g, 0.05 mol) in 100 ml benzene. During the addition, the temperature was allowed to rise to 50° C. and the triethylamine hydrochloride began to precipitate. After the addition was complete, the reaction was stirred an additional 30 minutes. The reaction was filtered and the filtrate evaporated in vacuo to give an oil which crystallized on cooling in an ice bath (m.p. 34°-35° C.). Benzene washings of the material retained on the filter paper gave a second fraction of oil which crystallized on cooling. Total yield was 11.97 g.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04478967 |
| Source dataset | uspto-grants-1984_10 |
| ORD ID | ord-a285f827b3314d6696a0c8ee1e2afecb |
| Source note | uspto-grants-1984_10 |