Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Formic Acid | HCID 284 | — |
| Reactant | Acetic Anhydride | HCID 7918 | — |
| Reactant | HCID 23322140 | HCID 23322140 | — |
| Solvent | Diethyl Ether | HCID 3283 | — |
| Product | HCID 23322137 | HCID 23322137 | — |
Reaction Steps
0.7 ml of acetic anhydride is added to 3 ml of 98% formic acid, kept at 0° C., and the whole is left for 15 minutes at 0° C. 2.2 g of 2-dipropylamino-7-amino-6-hydroxy-1,2,3,4-tetrahydronaphthalene hydrobromide are then added thereto and the mixture is then 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 |
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| Patent number | US04442126 |
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| Source dataset | uspto-grants-1984_04 |
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| ORD ID | ord-0e0de920bd6f4b4d802afd9b947a0b61 |
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| Source note | uspto-grants-1984_04 |
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