Dichloroacetyl chloride → HCID 53711305, compound
Reaction equation
[OH:1][N:2]=[C:3]([C:7]1[O:8][CH:9]=[CH:10][CH:11]=1)[C:4]([OH:6])=[O:5].[Cl:12][CH:13]([Cl:17])[C:14](Cl)=[O:15]>C(Cl)Cl>[Cl:12][CH:13]([Cl:17])[C:14]([O:1][N:2]=[C:3]([C:7]1[O:8][CH:9]=[CH:10][CH:11]=1)[C:4]([OH:6])=[O:5])=[O:15]Participants
4
Reactant 2
Product 1
Reagents, catalysts & solvents 1
Procedure
2-Hydroxyimino-2-(fur-2-yl)acetic acid (1.38 g) mixture was added portionwise to an ice cold solution of dichloroacetyl chloride (2 8 mls.) in dry methylene chloride (14 mls.). After 15 mins stirring a white precipitate was formed which was collected, washed successively with cold dry methylene chloride and petrol (b.p. 40-60°) and dried to yield 2-dichloroacetoxyimino-2-(fur-2-yl)acetic acid (syn-isomer) (1.5 g, 63%).
Workup
- customwas formed which
- customwas collected
- washwashed successively with cold dry methylene chloride and petrol (b.p. 40-60°)
- customdried
Sources & evidence
- ORD record
- ord-66cb770cd7ec4d72b0505b1417fe57cc
- Source dataset
- uspto-grants-1976_11
- Patent number
- US03991046
Reaction notes
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