tert-Butyl Formate → Tert-butyl 3-((2-cyano-3-nitrophenoxy)methyl)piperidine-1-carboxylate

HRID 471765

Reaction equation

HRID 471765 reaction equation
[OH:1][CH2:2][CH:3]1[CH2:8][CH2:7][CH2:6][N:5]([C:9]([O:11][C:12]([CH3:15])([CH3:14])[CH3:13])=[O:10])[CH2:4]1.[N+:16]([C:19]1[CH:26]=[CH:25][CH:24]=[C:23]([N+]([O-])=O)[C:20]=1[C:21]#[N:22])([O-:18])=[O:17].C(OC(C)(C)C)=O>>[C:21]([C:20]1[C:19]([N+:16]([O-:18])=[O:17])=[CH:26][CH:25]=[CH:24][C:23]=1[O:1][CH2:2][CH:3]1[CH2:8][CH2:7][CH2:6][N:5]([C:9]([O:11][C:12]([CH3:15])([CH3:14])[CH3:13])=[O:10])[CH2:4]1)#[N:22]

Participants

4

Procedure

Prepared as in Example 215c from tert-butyl 3-(hydroxymethyl)piperidine-1-carboxylate and 2,6-dinitrobenzonitrile in 58% yield. MS 263 [M+H-Boc]+.

Sources & evidence

ORD record
ord-4fb92bec1c964df2b1abbdab008f1545
Source dataset
uspto-grants-2014_01
Patent number
US08633186B2

Linked notes

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