HuagongsheHuagongshe Chemistry Print Report · For research reference only
Cetyl Alcohol → 1-Chloro-3-(hexadecyloxy)propan-2-ol
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Cetyl Alcohol | HCID 2682 | — |
| Reactant | Epichlorohydrin | HCID 7835 | — |
| Solvent | Diethyl Ether | HCID 3283 | — |
| Product | 1-Chloro-3-(hexadecyloxy)propan-2-ol | HCID 12458859 | 75% |
Reaction Steps
Hexadecanol (10.0 g, 0.0412 mole) and stannic chloride (0.04 g, 0.16 mmoles) were heated to 60° C. Epichlorohydrin (3.82 g, 0.0412 moles (was added over 1 hour and the reaction conditions kept constant for another hour. The hot product was extracted with 5% aqueous HCl and ether. The ether was concentrated to a white solid product (yield=75%).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US05206020 |
| Source dataset | uspto-grants-1993_04 |
| ORD ID | ord-dfa04e0bc3564c4584fadab6cf12931e |
| Source note | uspto-grants-1993_04 |