hydroxylamine-O-sulfonic acid → HCID 54021982, compound
Reaction equation
[N+:1]([C:4]1[CH:5]=[C:6]([CH:18]=[CH:19][CH:20]=1)[CH2:7][N:8]1[CH:12]=[C:11]([CH2:13][CH2:14][C:15](O)=[O:16])[N:10]=[N:9]1)([O-:3])=[O:2].NOS(O)(=O)=O.[N+](C1C=C(C=CC=1)CN1C=C(C=CC(O)=O)N=N1)([O-])=O>>[N+:1]([C:4]1[CH:5]=[C:6]([CH:18]=[CH:19][CH:20]=1)[CH2:7][N:8]1[CH:12]=[C:11]([CH:13]=[CH:14][CH:15]=[O:16])[N:10]=[N:9]1)([O-:3])=[O:2]Participants
4
Procedure
3-[1-(3-nitrobenzyl)-1,2,3-triazol-4-yl]-propionic acid (m.p. 147°-150° C.; prepared by reduction by means of hydroxylamine-O-sulphonic acid of 3-[1-(3-nitrobenzyl)-1,2,3-triazol-4-yl]-acrylic acid (m.p. 155°-158° C.), which is obtained by oxidation of the corresponding 3-[1-(3-nitrobenzyl)-1,2,3-triazol-4-yl]-acrolein (m.p. 136°-140° C.):
Sources & evidence
- ORD record
- ord-c38af45d8c8949a08506bae42aea1f0f
- Source dataset
- uspto-grants-1987_08
- Patent number
- US04687767
Reaction notes
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