5-Chloro-2-furaldehyde → HCID 59054303, compound

HRID 1400253Notes

Reaction equation

HRID 1400253 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[O:23][C:22]([CH:24]=O)=[CH:21][CH:20]=1>>[Cl:18][C:19]1[O:23][C:22]([CH2:24][NH:16][C:14]([CH3:17])([CH3:15])[CH2:13][O:12][C:3]2[CH:4]=[CH:5][C:6]3[C:11](=[CH:10][CH:9]=[CH:8][CH:7]=3)[C:2]=2[Cl:1])=[CH:21][CH:20]=1

Participants

3

Reactant 2

HCID 27696305-Chloro-2-furaldehydeHCID 681517291-[(1-Chloro-2-naphthalenyl)oxy]-2-methyl-2-propanamine

Product 1

HCID 59054303HCID 59054303, compoundYield 32%

Procedure

Prepared from 1-[(1-chloronaphthalen-2-yl)oxy]-2-methylpropan-2-amine and 5-chlorofuran-2 carbaldehyde in 32% yield as a yellow oil.

Sources & evidence

ORD record
ord-17035b417fdc429fb46214d7d5c2cb85
Source dataset
uspto-grants-2014_12
Patent number
US08906946B2

Reaction notes

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