HuagongsheHuagongshe Chemistry Print Report · For research reference only
Stearoyl chloride → HCID 15095407, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Stearoyl chloride | HCID 8212 | — |
| Reactant | Triethylamine | HCID 8471 | — |
| Reactant | 2-Nitrobenzyl alcohol | HCID 11923 | — |
| Solvent | Benzene | HCID 241 | — |
| Product | HCID 15095407 | HCID 15095407 | — |
Reaction Steps
In 100 ml benzene were mixed 2-nitrobenzyl alcohol (7.65 g, 0.05 mol) and triethylamine (5.06 g, 0.05 mol). To the solution octadecanoyl chloride (15.14 g, 0.05 mol) was added dropwise with stirring. The mixture was stirred an additional one hour and the precipitated triethyl amine hydrochloride was removed by filtration. The filtrate was evaporated to dryness and the residue crystallized from ethanol (yield 13.0 g, m.p. 60°-61° C.). The tetradecanoate (m.p. 46° C.) (Compound 5), hexadecanoate (m.p. 54° C.) (Compound 6), heptadecanoate (m.p. 48° C.) (Compound 7), and 9-octadecenoate (Compound 8) esters of 2-nitrobenzyl alcohol were similarly prepared using corresponding acyl chlorides in place of octadecanoyl chloride.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04980096 |
| Source dataset | uspto-grants-1990_12 |
| ORD ID | ord-b62e655f84954ceeb707324376b49c77 |
| Source note | uspto-grants-1990_12 |