HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1757809Generated: October 31, 2026
Benzyl Alcohol → 3-(Octadecyloxy)-5-(3-phenoxypropoxy)phenylcarbamic acid phenylmethyl ester
https://huagongshe.com/reaction/1757809
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Benzyl Alcohol | HCID 244 | — |
| Reactant | Triethylamine | HCID 8471 | — |
| Reactant | P,P-Diphenylphosphinic azide | HCID 199401 | — |
| Reactant | 3-(Octadecyloxy)-5-(3-phenoxypropoxy)benzoic acid | HCID 15232834 | — |
| Solvent | Toluene | HCID 1140 | — |
| Product | 3-(Octadecyloxy)-5-(3-phenoxypropoxy)phenylcarbamic acid phenylmethyl ester | HCID 15232835 | 85% |
Reaction Steps
To a suspension of 10.7 g (0.02 mol) 3-(octadecyloxy)-5-(3-phenoxypropoxy)benzoic acid in 250 ml of anhydrous toluene cooled in an ice bath was added 5.1 ml (0.024 mol) of diphenylphosphoryl azide followed by 3.8 ml (0.028 mol) of triethylamine. The reaction mixture was stirred in an ice bath for 1 hour and then heatedat 90° for 2 hours. After cooling to room temperature, 70 ml of benzyl alcohol was added. The reaction mixture was then stirred and heatedat 90° for 18 hours. The solvent was removed at reduced pressure andthe residue was dissolved in ethyl acetate. The extract was washed with saturated NaHCO3 solution, dried and concentrated to an oil which waspurified by HPLC using 10% ethyl acetate-hexane to give 10.9 g (85% yield, mp 68°-69°) of 3-(octadecyloxy)-5-(3-phenoxypropoxy)phenylcarbamic acid phenylmethyl ester. The structure was confirmed by nmr and mass spectra.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|
| Patent number | US05446189 |
|---|
| Source dataset | uspto-grants-1995_08 |
|---|
| ORD ID | ord-609021a419a64ef1b3d427c4b6830b68 |
|---|
| Source note | uspto-grants-1995_08 |
|---|