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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1858838Generated: November 2, 2026

Trifluoroacetic acid → HCID 69646414, compound

https://huagongshe.com/reaction/1858838

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTrifluoroacetic acidHCID 6422—
ReactantHCID 86604514HCID 86604514—
ProductHCID 69646414HCID 69646414—

Reaction Steps

In an analogous manner to that described in Example 145(i), from tert-butyl (3'RS,4'RS)-4-(3-benzyloxy-propoxy)-3'-(naphthalen-2-ylmethoxy)-2-oxo-3',4',5',6'-tetrahydro-2H,2'H-[1,4']bipyridine-1'-carboxylate by cleavage of the BOC group by means of trifluoroacetic acid there was obtained (3'RS,4'RS)-4-(3-benzyloxy-propoxy)-3'-(naphthalen-2-ylmethoxy)-1',2',3',4',5',6'-hexahydro-[1,4']bipyridin-2-one trifluoroacetate as a colourless solid; MS: 499 (M+H)+.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06150526
Source datasetuspto-grants-2000_11
ORD IDord-4095c57cfa0a4db1989c9f8660c5bcea
Source noteuspto-grants-2000_11