4-Iodoaniline → HCID 12343653, compound

HRID 2198864

Reaction equation

[I:1][C:2]1[CH:8]=[CH:7][C:5]([NH2:6])=[CH:4][CH:3]=1.Br[CH:10]([C:14]1[CH:19]=[CH:18][CH:17]=[CH:16][CH:15]=1)[C:11]([NH2:13])=[O:12]>>[I:1][C:2]1[CH:8]=[CH:7][C:5]([NH:6][CH:10]([C:14]2[CH:19]=[CH:18][CH:17]=[CH:16][CH:15]=2)[C:11]([NH2:13])=[O:12])=[CH:4][CH:3]=1

Participants

Reactant 2

HCID 108934-Iodoaniline

HCID 2420282-Bromo-2-phenylacetamide

Product 1

HCID 12343653HCID 12343653, compound

Procedure

In accordance with the procedure of example 4 p-iodoaniline and α-bromophenylacetamide were reacted to yield α-(p-iodoanilino)phenylacetamide, Rf =0.65.

Sources & evidence

ORD record: ord-f3c3b829c42a4a3f983d5bd509935d4a
Source dataset: uspto-grants-1982_11
DOI: 10.6084/m9.figshare.5104873.v1
Patent number: US04360511

Linked notes

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