4-Hydroxybenzaldehyde → HCID 67061110, compound

HRID 401090Notes

Reaction equation

HRID 401090 reaction equation
[OH:1][C:2]1[CH:9]=[CH:8][C:5]([CH:6]=O)=[CH:4][CH:3]=1.[C:10]1([C:16](=O)[CH2:17][C:18]2[CH:23]=[CH:22][CH:21]=[CH:20][CH:19]=2)[CH:15]=[CH:14][CH:13]=[CH:12][CH:11]=1.[NH2:25][C:26]([NH2:28])=[O:27]>C(O)(=O)C>[OH:1][C:2]1[CH:9]=[CH:8][C:5]([CH:6]2[C:17]([C:18]3[CH:23]=[CH:22][CH:21]=[CH:20][CH:19]=3)=[C:16]([C:10]3[CH:15]=[CH:14][CH:13]=[CH:12][CH:11]=3)[NH:28][C:26](=[O:27])[NH:25]2)=[CH:4][CH:3]=1

Participants

5

Reactant 3

HCID 1264-HydroxybenzaldehydeHCID 1176UreaHCID 99482-Phenylacetophenone

Product 1

HCID 67061110HCID 67061110, compound

Reagents, catalysts & solvents 1

HCID 176Acetic AcidSolvent

Procedure

Followed the procedure described in Example 86, starting from 4-hydroxybenzaldehyde, 1,2-diphenylethanone and urea, and acetic acid was used instead of HCl.

Sources & evidence

ORD record
ord-f56a1e9e36bb43af8becf95c75c4896b
Source dataset
uspto-grants-2014_06
Patent number
US08741915B2

Reaction notes

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