HuagongsheHuagongshe Chemistry Print Report · For research reference only
Acetic Anhydride → N-{4-[(Oxan-2-yl)oxy]nonyl}acetamide
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Acetic Anhydride | HCID 7918 | — |
| Reactant | 4-(2-Tetrahydropyranyloxy)nonylamine | HCID 20327684 | — |
| Solvent | Pyridine | HCID 1049 | — |
| Product | N-{4-[(Oxan-2-yl)oxy]nonyl}acetamide | HCID 21503928 | — |
Reaction Steps
To a stirred, ice cold solution of 4-(2-tetrahydropyranyloxy)nonylamine (7.29 g., 0.03 mole) in pyridine (40 ml.) is added acetic anhydride (3.06 g., 0.03 mole) at such a rate as to maintain the reaction temperature at 5°-10°C. The reaction is then allowed to stand at room temperature for 6 hours, poured into ice water (200 ml.) and extracted with ether (2 × 100 ml.). The ether is extracted with ice cold 5% hydrochloric acid (2 × 20 ml.), washed with brine (2 × 25 ml.), then dried over sodium sulfate. Evaporation in vacuo affords the subject compound as a pale yellow oil.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US03987091 |
| Source dataset | uspto-grants-1976_10 |
| ORD ID | ord-76b123cd98964ac4b1f91c6f6c15d31a |
| Source note | uspto-grants-1976_10 |