Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Formic Acid | HCID 284 | — |
| Reactant | Acetic Anhydride | HCID 7918 | — |
| Reactant | HCID 23322139 | HCID 23322139 | — |
| Solvent | Diethyl Ether | HCID 3283 | — |
| Product | HCID 23322136 | HCID 23322136 | — |
Reaction Steps
0.42 ml of acetic anhydride is added all at once to 2 ml of 98% formic acid, kept at 0° C., and the mixture is left at 0° C. for 15 minutes. Then, still using an ice-bath, 1.34 g of 2-dipropylamino-5-amino-6-hydroxy-1,2,3,4-tetrahydronaphthalene hydrobromide are introduced therein with a spatula and the whole is stirred for one hour at 0° C. After 50 ml of diethyl ether have been added and the solid has been filtered off, the latter is recrystallised from a 50/50 methanol/ethyl acetate mixture. This gives 1 g of the final product melting at 213° C. (with decomposition).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|
| Patent number | US04520030 |
|---|
| Source dataset | uspto-grants-1985_05 |
|---|
| ORD ID | ord-2beadab662ae4f6cb16ae19f7b9463fb |
|---|
| Source note | uspto-grants-1985_05 |
|---|