HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1156693Generated: November 1, 2026
Isoproterenone hydrochloride → HCID 54097762, compound
https://huagongshe.com/reaction/1156693
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Isoproterenone hydrochloride | HCID 2830496 | — |
| Reactant | Octadeca-10,13-dienoyl chloride | HCID 53680516 | — |
| Product | HCID 54097762 | HCID 54097762 | — |
Reaction Steps
Following the procedure described above in Example 58A but using 3,4-dihydroxyphenyl isopropylaminomethyl ketone hydrochloride instead of 3,4-dihydroxyphenyl tert-butylaminomethyl ketone hydrochloride and 10,13-octadecadienoyl chloride instead of isovaleryl chloride, there is obtained 3-hydroxy-4-(10,13-octadecadienoyloxy)phenyl isopropylaminomethyl ketone; and by interaction of this base with methanesulfonic acid there is obtained the methanesulfonate salt. When this methanesulfonate is reduced with sodium borohydride, using a procedure similar to that described above in Example 30C, there is obtained 3-hydroxy-4-(10,13-octadecadienoyloxy)-alpha-(isopropylaminomethyl)benzyl alcohol methanesulfonate. By catalytic hydrogenation of 3-hydroxy-4-(10,13-octadienoyloxy)phenyl isopropylaminomethyl ketone methanesulfonate, using a procedure similar to that described above in Example 30B, there is obtained 3-hydroxy-4-(octadecanoyloxy)-alpha-(isopropylaminomethyl)benzyl methanesulfonate.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US04336400 |
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| Source dataset | uspto-grants-1982_06 |
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| ORD ID | ord-b429bf235ed64f5cb48b8dddb848ab3c |
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| Source note | uspto-grants-1982_06 |
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