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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1390460Generated: November 2, 2026

Nicotinoyl chloride → 3-(Nicotinoyloxy)-4-(p-toluyloxy)phenyl tert-butylaminomethyl ketone

https://huagongshe.com/reaction/1390460

Reaction equation

Participants

RoleNameHCIDCharge
ReactantNicotinoyl chlorideHCID 82604—
Reactant3-Hydroxy-4-(p-toluyloxy)phenyl tert-butylaminomethyl ketoneHCID 54189973—
Product3-(Nicotinoyloxy)-4-(p-toluyloxy)phenyl tert-butylaminomethyl ketoneHCID 53663371—

Reaction Steps

Following a procedure similar to that described above in Example 30A, when 3-hydroxy-4-(p-toluyloxy)phenyl tert-butylaminomethyl ketone is interacted with nicotinoyl chloride, there is obtained 3-(nicotinoyloxy)-4-(p-toluyloxy)phenyl tert-butylaminomethyl ketone; and by interaction of this base with hydrochloric acid there is obtained the hydrochloride salt. When this hydrochloride is catalytically hydrogenated, using the procedure described above in Example 30B, there is obtained 3- nicotinoyloxy-4-(p-toluyloxy)-alpha-(tert-butylaminomethyl) benzyl alcohol hydrochloride.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04138581
Source datasetuspto-grants-1979_02
ORD IDord-1a1a1efca24d4248b504965d6d1454b2
Source noteuspto-grants-1979_02