HuagongsheHuagongshe Chemistry Print Report · For research reference only
Stearyl Alcohol → HCID 17957563, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Stearyl Alcohol | HCID 8221 | — |
| Reactant | Benzenesulfonic acid, 4-methyl-, compd. with pyridine (1:1) | HCID 466102 | — |
| Reactant | HCID 17957558 | HCID 17957558 | — |
| Solvent | Cyclohexane | HCID 8078 | — |
| Product | HCID 17957563 | HCID 17957563 | — |
Reaction Steps
3 g of 2,2,2-trifluoro-N-(2-methoxy-[1,3]dioxolan-4-ylmethyl)acetamide (Ortho 1, 13.09 mmol) were mixed with 3.54 g of octadecanol (13.09 mmol). The mixture was melted at 80° C. and left for 2 hours after the addition of 32 mg of pyridinium para-toluenesulfonate (0.13 mmol). The crude reaction product was then dissolved in cyclohexane, washed with a saturated sodium hydrogen carbonate solution and then with a saturated sodium chloride solution, dried over magnesium. sulfate and then concentrated to dryness. This crude product was used as it was for the next step.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US07641914B2 |
| Source dataset | uspto-grants-2010_01 |
| ORD ID | ord-b8dd7a59e3664098aec2facfbec18648 |
| Source note | uspto-grants-2010_01 |