2-Thiophenecarboxaldehyde, 5-chloro- → HCID 59054376, compound

HRID 1400261Notes

Reaction equation

HRID 1400261 reaction equation
[Cl:1][C:2]1[C:11]2[C:6](=[CH:7][CH:8]=[CH:9][CH:10]=2)[CH:5]=[CH:4][C:3]=1[O:12][CH:13]([CH3:16])[CH2:14][NH2:15].[Cl:17][C:18]1[S:22][C:21]([CH:23]=O)=[CH:20][CH:19]=1>>[Cl:1][C:2]1[C:11]2[C:6](=[CH:7][CH:8]=[CH:9][CH:10]=2)[CH:5]=[CH:4][C:3]=1[O:12][CH:13]([CH3:16])[CH2:14][NH:15][CH2:23][C:21]1[S:22][C:18]([Cl:17])=[CH:19][CH:20]=1

Participants

3

Reactant 2

HCID 817002-Thiophenecarboxaldehyde, 5-chloro-HCID 68151505HCID 68151505, compound

Product 1

HCID 59054376HCID 59054376, compoundYield 69%

Procedure

Prepared from 2-[(1-chloronaphthalen-2-yl)oxy]propan-1-amine and 5-chlorothiophen-2-carbaldehyde in 69% yield as a yellow oil.

Sources & evidence

ORD record
ord-6b01ec51eea44d7587fa538290f4d4a4
Source dataset
uspto-grants-2014_12
Patent number
US08906946B2

Reaction notes

Loading…