Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Sodium Acetate | HCID 517045 | — |
| Reactant | HCID 13728033 | HCID 13728033 | — |
| Solvent | Acetic Anhydride | HCID 7918 | — |
| Product | HCID 20212691 | HCID 20212691 | — |
Reaction Steps
A mixture of 2.21 g of the carboxyl compound obtained in Example 8 and 0.45 g of sodium acetate in 10 ml of acetic anhydride was heated at 100° C. for 2 hours, and the mixture was concentrated under reduced pressure. n-Hexane was added to the mixture and the insoluble matter was filtered off. The filtrate was concentrated to dryness to give a crude product of 3-octadecyloxy-2-succinimido-1-trityloxypropanol. This crude trityl compound in 20 ml of 70% acetic acid was heated at 100° C. for 2 hours. The reaction mixture was concentrated to dryness and the residue was purified by silica gel chromatography (chloroform-methanol=20:1) to give 1.316 g (95%) of the desired compound as a colorless powder.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|
| Patent number | US04650791 |
|---|
| Source dataset | uspto-grants-1987_03 |
|---|
| ORD ID | ord-74834b4f4f924976a9514a22a71e44af |
|---|
| Source note | uspto-grants-1987_03 |
|---|