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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1156693Generated: November 1, 2026

Isoproterenone hydrochloride → HCID 54097762, compound

https://huagongshe.com/reaction/1156693

Reaction equation

Participants

RoleNameHCIDCharge
ReactantIsoproterenone hydrochlorideHCID 2830496—
ReactantOctadeca-10,13-dienoyl chlorideHCID 53680516—
ProductHCID 54097762HCID 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

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04336400
Source datasetuspto-grants-1982_06
ORD IDord-b429bf235ed64f5cb48b8dddb848ab3c
Source noteuspto-grants-1982_06