HuagongsheHuagongshe Chemistry Print Report · For research reference only
Acetic Anhydride → HCID 20522156, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Acetic Anhydride | HCID 7918 | — |
| Reactant | HCID 178451644 | HCID 178451644 | — |
| Solvent | Chloroform | HCID 6212 | — |
| Product | HCID 20522156 | HCID 20522156 | — |
Reaction Steps
t-BOC THIP (7.2 g) was refluxed with acetic acid anhydride (5.0 g) in 50 ml of CHCl3 for 2 hours. 2-Acetyl-6-(t-butyloxycarbonyl)-4,5,6,7-tetrahydroisoxazolo[5,4-c]pyridine-3-one was isolated as an oil in 6.4 g (76%) yield by column chromatography (Silicagel 60 "Merck") (eluted with ether/CH2Cl2 (1:3)). The t-BOC group was split off as above, yielding 73% of the oxalate. M.P. 177°-178° C. (dec.) (Found: C 44.32; H 4.70; N (10.58); C10H12N2O7 requires C 44.12; H 4.45; N 10.29%).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04353910 |
| Source dataset | uspto-grants-1982_10 |
| ORD ID | ord-35e522618d254a7699b9d4b947aecd5d |
| Source note | uspto-grants-1982_10 |