Hydroxyacetonitrile → HCID 21430687, compound
Reaction equation
[C:1](#[N:4])[CH2:2][OH:3].[N+:5]([C:8]1[CH:9]=[C:10]([S:14](Cl)(=[O:16])=[O:15])[CH:11]=[CH:12][CH:13]=1)([O-:7])=[O:6]>>[N+:5]([C:8]1[CH:9]=[C:10]([S:14]([O:3][CH2:2][C:1]#[N:4])(=[O:16])=[O:15])[CH:11]=[CH:12][CH:13]=1)([O-:7])=[O:6]Participants
3
Procedure
Preparation: The technique of Example 2 is used to react glycolonitrile with m-nitrobenzenesulfonyl chloride. The product is recovered from the reaction mixture by filtration and recrystallized from ethanol. The dried product (45% conversion) is an amber solid, m.p. 66°-69° C.
Workup
- customPreparation
- filtrationThe product is recovered from the reaction mixture by filtration
- customrecrystallized from ethanol
Sources & evidence
- ORD record
- ord-37e1a7393f2e4ef3a7dad24bde78bc32
- Source dataset
- uspto-grants-1977_06
- Patent number
- US04029809
Reaction notes
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