HuagongsheHuagongshe Chemistry Print Report · For research reference only
Hydrogen Bromide → HCID 12390942, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Hydrogen Bromide | HCID 260 | — |
| Reactant | HCID 12390947 | HCID 12390947 | — |
| Reactant | HCID 20316899 | HCID 20316899 | — |
| Product | HCID 12390942 | HCID 12390942 | — |
Reaction Steps
20 Parts of 2-amino-5,6-dibenzyloxy-3,4-dihydro-1(2H)-naphthalenone hydrochloride is subjected to a procedure similar to that described in Reference Example 11 and the resultant 5,6-dibenzyloxy-2-trifluoroacetamido-3,4-dihydro-1(2H)-naphthalenone is reacted with 60 parts of 3-phenylpropanol p-toluenesulfonic acid ester under the same conditions as set forth in Reference Example 11. The reaction product is then hydrolyzed in a 47% aqueous solution of hydrogen bromide to obtain 3 parts of 5,6-dihydroxy-2-(3-phenylpropylamino)-3,4-dihydro-1(2H)-naphthalenone hydrobromide melting at 215°-217° C (decomposition).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04104402 |
| Source dataset | uspto-grants-1978_08 |
| ORD ID | ord-c6a7b5497e67496e8fc9d7bafcf5db0d |
| Source note | uspto-grants-1978_08 |