2-Naphthalenecarboxaldehyde → HCID 2794958, compound

HRID 1402953Notes

Reaction equation

[CH:1]1[C:10]2[C:5](=[CH:6][CH:7]=[CH:8][CH:9]=2)[CH:4]=[CH:3][C:2]=1[CH:11]=[O:12].[C:13]([C:16]1[CH:25]=[CH:24][C:23]2[C:18](=[CH:19][CH:20]=[CH:21][CH:22]=2)[CH:17]=1)(=O)[CH3:14]>>[CH:1]1[C:10]2[C:5](=[CH:6][CH:7]=[CH:8][CH:9]=2)[CH:4]=[CH:3][C:2]=1[C:11](=[O:12])[CH:14]=[CH:13][C:16]1[CH:25]=[CH:24][C:23]2[C:18](=[CH:19][CH:20]=[CH:21][CH:22]=2)[CH:17]=1

Participants

Reactant 2

HCID 62012-Naphthalenecarboxaldehyde

HCID 71222-Acetylnaphthalene

Product 1

HCID 2794958HCID 2794958, compound

Procedure

By a procedure similar to that of example 1.59.1, starting from 2-naphthaldehyde and 2-acetylnaphthalene, 1,3-di-(2-naphthalenyl)prop-2-en-1-one was obtained as yellow solid.

Sources & evidence

ORD record: ord-d8f7e1a44ba748aba0512a4d0313fb88
Source dataset: uspto-grants-2014_12
DOI: 10.6084/m9.figshare.5104873.v1
Patent number: US08912186B2

Reaction notes

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