Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1156680Generated: October 31, 2026

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

https://huagongshe.com/reaction/1156680

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 numberUS04336400
Source datasetuspto-grants-1982_06
ORD IDord-e9fdb80045194a9db7152a23be254b48
Source noteuspto-grants-1982_06