HuagongsheHuagongshe Chemistry Print Report · For research reference only
Chloroform → Acetate
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Chloroform | HCID 6212 | — |
| Reactant | Propionic anhydride | HCID 31263 | — |
| Reactant | Acetic acid 10-acetoxymethyl-anthracen-9-ylmethyl ester | HCID 613145 | — |
| Solvent | Pyridine | HCID 1049 | — |
| Product | Acetate | HCID 175 | — |
| Product | Benzoate | HCID 242 | — |
| Product | Propionate ion | HCID 104745 | — |
| Product | HCID 6931746 | HCID 6931746 | — |
Reaction Steps
Starting from a 5α-alkoxymethyl-2β,4α-dihydroxycyclopentyl-1β-acetic acid-γ-lactone, wherein the alkoxy group is a methoxy, benzyloxy and p-methoxybenzyloxy group, esterification in pyridine with 1.3 molar equivalents of both acetic, acetic-formic or propionic anhydride and benzoyl or p-phenylbenzoyl chloride, gave the 4α-formate, acetate, m.p. 76-77°, [α]D = -29.5°, [α]365° = -74° (CHCl3), propionate, benzoate and p-phenylbenzoate.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04133829 |
| Source dataset | uspto-grants-1979_01 |
| ORD ID | ord-b19267b85e61439fbc39f8a58b515f75 |
| Source note | uspto-grants-1979_01 |