HuagongsheHuagongshe Chemistry Print Report · For research reference only
Acetic Acid → Acetic Anhydride
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Acetic Acid | HCID 176 | — |
| Reactant | HCID 178475128 | HCID 178475128 | — |
| Product | Acetic Anhydride | HCID 7918 | — |
| Product | HCID 178514283 | HCID 178514283 | — |
Reaction Steps
Mixed anhydride of acetic acid and 6-(2-carboxyethyl)-3-mercapto-4-acetamino-1,2,4-triazin-5-one. The vacuum dried (55° C., 0.05 mm, 4 hours) product obtained from the reaction of acetic anhydride and 6-(2-carboxyethyl)-3-mercapto-4-amino-1,2,4-triazin-5-one at 145° C. (bath temperature) for 8 hours as described in Example 1 (but not reacted with t-butanol) is separated. Mp. 95°-100° C.; dec. 130° C. Insoluble in water, alcohol, and t-butyl alcohol; soluble in acetone, chloroform, and acetonitrile. Anal. Calcd. for C14H20O5N4S: N, 20.59; S, 11.76. Found: N, 20.56; S, 11.68.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04405779 |
| Source dataset | uspto-grants-1983_09 |
| ORD ID | ord-9fdc5e5e4df74e0f9a910e0ec7cdd2db |
| Source note | uspto-grants-1983_09 |