HuagongsheHuagongshe Chemistry Print Report · For research reference only
Acetic Anhydride → 2-Pyrrolidineethanol, alpha-(3-methoxyphenyl)-1-methyl-, acetate (ester), (R*,S*)-
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Acetic Anhydride | HCID 7918 | — |
| Reactant | Sodium Hydroxide | HCID 14798 | — |
| Reactant | 2-Pyrrolidineethanol, alpha-(3-methoxyphenyl)-1-methyl-, (R*,S*)- | HCID 3054350 | — |
| Product | 2-Pyrrolidineethanol, alpha-(3-methoxyphenyl)-1-methyl-, acetate (ester), (R*,S*)- | HCID 3054358 | — |
Reaction Steps
3,5 g of (R*,S*)-1-(3-methoxyphenyl)-2-(1-methyl-2-pyrrolidinyl)-ethanol and 40 ml of acetic acid anhydride are stirred for 15 minutes at room temperature. 6 N sodium hydroxide solution is added with cooling up to a pH of 8-9. The mixture is extracted with diethyl ether, and the organic layer is concentrated to the oily title compound. The hydrochloride (from methanol/diethyl ether) melts at 155°-157°.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04198424 |
| Source dataset | uspto-grants-1980_04 |
| ORD ID | ord-0c2a1dc78aa24b82a0a9768b7b939603 |
| Source note | uspto-grants-1980_04 |