Thionyl Chloride → HCID 86621811, compound

HRID 1643343Notes

Reaction equation

[CH2:1]([O:8][C:9]1[CH:17]=[C:16]([O:18][CH2:19][C:20]2[CH:25]=[CH:24][CH:23]=[CH:22][CH:21]=2)[C:15]([S:26](=[O:33])(=[O:32])[N:27]([CH3:31])[CH2:28][CH2:29][CH3:30])=[CH:14][C:10]=1[C:11](O)=[O:12])[C:2]1[CH:7]=[CH:6][CH:5]=[CH:4][CH:3]=1.S(Cl)([Cl:36])=O>>[CH2:1]([O:8][C:9]1[CH:17]=[C:16]([O:18][CH2:19][C:20]2[CH:25]=[CH:24][CH:23]=[CH:22][CH:21]=2)[C:15]([S:26](=[O:33])(=[O:32])[N:27]([CH3:31])[CH2:28][CH2:29][CH3:30])=[CH:14][C:10]=1[C:11]([Cl:36])=[O:12])[C:2]1[CH:7]=[CH:6][CH:5]=[CH:4][CH:3]=1

Participants

Reactant 2

HCID 24386Thionyl Chloride

HCID 66756617HCID 66756617, compound

Product 1

HCID 86621811HCID 86621811, compound

Procedure

2.9 Reaction of 2,4-dibenzyloxy-5-(N-methyl-N-propylsulfamoyl)benzoic acid with thionyl chloride gives the compound 2,4-dibenzyloxy-5-(N-methyl-N-propylsulfamoyl)benzoyl chloride.

Sources & evidence

ORD record: ord-17f11f9dab7649d4b3834830c09cd9e2
Source dataset: uspto-grants-2012_02
DOI: 10.6084/m9.figshare.5104873.v1
Patent number: US08119795B2

Reaction notes

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