HCID 11427452, compound → HCID 23134889, compound

HRID 1437835Notes

Reaction equation

HRID 1437835 reaction equation
[Cl:1][C:2]1[C:3]([OH:16])=[C:4]([CH:12]([OH:15])[CH2:13][CH3:14])[C:5]([OH:11])=[C:6]([C:9]=1[CH3:10])[CH:7]=[O:8].Cl[C:18]1[C:19](O)=[C:20]([CH:28](O)[CH2:29][CH2:30][CH2:31]C)C(O)=[C:22]([C:25]=1C)C=O.ClC1C(O)=C(C(O)CCCCCC)C(O)=C(C=1C)C=O.ClC1C(O)=C(C(O)CCCCCCCC)C(O)=C(C=1C)C=O.ClC1C(O)=C(C(O)CCCCCCCCC)C(O)=C(C=1C)C=O>>[Cl:1][C:2]1[C:3]([OH:16])=[C:4]([CH:12]([OH:15])[CH2:13][CH2:14][CH2:22][CH2:25][CH2:18][CH2:19][CH2:20][CH2:28][CH2:29][CH2:30][CH3:31])[C:5]([OH:11])=[C:6]([C:9]=1[CH3:10])[CH:7]=[O:8]

Participants

6

Reactant 5

HCID 11427452HCID 11427452, compoundHCID 23134876HCID 23134876, compoundHCID 23134880HCID 23134880, compoundHCID 23134882HCID 23134882, compoundHCID 23134896HCID 23134896, compound

Product 1

HCID 23134889HCID 23134889, compound

Procedure

In addition to this compound, 5-chloro-2,4-dihydroxy-3-(1-hydroxypropyl)-6-methylbenzaldehyde (196-3), 5-chloro-2,4-dihydroxy-3-(1-hydroxypentyl)-6-methylbenzaldehyde (196-5), 5-chloro-2,4-dihydroxy-3-(1-hydroxyheptyl)-6-methylbenzaldehyde (196-7), 5-chloro-2,4-dihydroxy-3-(1-hydroxynonyl)-6-methylbenzaldehyde (196-9) and 5-chloro-2,4-dihydroxy-3-(1-hydroxydecyl)-6-methylbenzaldehyde (196-10) were synthesized by the same reaction with the use of respective corresponding starting raw materials.

Workup

  1. customwere synthesized by the same reaction with the use of respective

Sources & evidence

ORD record
ord-8e4b951315a34c96802a6813a31497e8
Source dataset
uspto-grants-2009_11
Patent number
US07622598B2

Reaction notes

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