4-Nitrophenol → HCID 19888357, compound

HRID 654085Notes

Reaction equation

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

Participants

Reactant 2

HCID 9804-Nitrophenol

HCID 19888362HCID 19888362, compound

Product 1

HCID 19888357HCID 19888357, compound

Procedure

The title compound is prepared according to the procedures of Example 3 from 1-(1-phenylethyl)-3-azetidine ethanol and 4-nitrophenol.

Sources & evidence

ORD record: ord-194b9288cd604a7aad76aea6354bfd3c
Source dataset: uspto-grants-1992_07
DOI: 10.6084/m9.figshare.5104873.v1
Patent number: US05130309

Reaction notes

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