HuagongsheHuagongshe Chemistry Print Report · For research reference only
Triethylamine → 2-Nitrobenzyl hexadecanesulfonate
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Triethylamine | HCID 8471 | — |
| Reactant | 2-Nitrobenzyl alcohol | HCID 11923 | — |
| Reactant | 1-Hexadecanesulfonyl chloride | HCID 96923 | — |
| Solvent | Benzene | HCID 241 | — |
| Product | 2-Nitrobenzyl hexadecanesulfonate | HCID 15095411 | — |
Reaction Steps
To a stirred solution of 7.65 g (0.05 mol) of 2-nitrobenzyl alcohol in 75 ml of benzene containing 5.05 g (0.05 ml) of triethylamine was added 16.25 g (0.05 mol of hexadecanesulfonyl chloride. The mixture was stirred an additional four hours. The mixture was evaporated to dryness in vacuo and the solid taken up into a mixture of ether and water. The ether layer was separated and dried over MgSO4. Evaporation of the ether gave a solid which was crystallized from absolute ethanol (yield 14.3 g, m.p. 63°-65° C.).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04599273 |
| Source dataset | uspto-grants-1986_07 |
| ORD ID | ord-a736dbcfcc3b4614b9151afa12419af4 |
| Source note | uspto-grants-1986_07 |