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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1156710Generated: November 1, 2026

Methanesulfonic Acid → HCID 54532739, compound

https://huagongshe.com/reaction/1156710

Reaction equation

Participants

RoleNameHCIDCharge
ReactantMethanesulfonic AcidHCID 6395—
ReactantSodium borohydrideHCID 4311764—
ReactantHCID 70553942HCID 70553942—
SolventMethanolHCID 887—
ProductHCID 54532739HCID 54532739—

Reaction Steps

Proceeding in a manner similar to that described above in part B of Example 151, 22 g. of 3-(acetoxymethyl)-4-(o-toluyloxy)phenyl tert-butylaminomethyl ketone hydrochloride was reduced in anhydrous methyl alcohol with 1.13 g. of sodium borohydride and the reduction product was treated with methanesulfonic acid to yield 3-(acetoxymethyl)-4-(o-toluyloxy)-alpha-(tert-butylaminomethyl)benzyl alcohol methanesulfonate as a white solid which melted at 116°-118° C. (uncorr.).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04336400
Source datasetuspto-grants-1982_06
ORD IDord-19f6a5809e7c406388609e6ccff2ff24
Source noteuspto-grants-1982_06