2-Thiophenecarboxaldehyde, 5-chloro- → HCID 59054304, compound

HRID 1400254Notes

Reaction equation

HRID 1400254 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][CH2:13][C:14]([CH3:17])([NH2:16])[CH3:15].[Cl:18][C:19]1[S:23][C:22]([CH:24]=O)=[CH:21][CH:20]=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][CH2:13][C:14]([CH3:17])([NH:16][CH2:24][C:22]1[S:23][C:19]([Cl:18])=[CH:20][CH:21]=1)[CH3:15]

Participants

3

Reactant 2

HCID 817002-Thiophenecarboxaldehyde, 5-chloro-HCID 681517291-[(1-Chloro-2-naphthalenyl)oxy]-2-methyl-2-propanamine

Product 1

HCID 59054304HCID 59054304, compoundYield 29%

Procedure

Prepared from 1-[(1-chloronaphthalen-2-yl)oxy]-2-methylpropan-2-amine and 5-chlorothiophen-2 carbaldehyde in 29% yield as a brown oil.

Sources & evidence

ORD record
ord-f0694c7513044aab89a80fcbd84927a9
Source dataset
uspto-grants-2014_12
Patent number
US08906946B2

Reaction notes

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