Isobutyryl chloride → HCID 22034976, compound
Reaction equation
[C:1](Cl)(=[O:5])[CH:2]([CH3:4])[CH3:3].[CH3:7][O:8][CH:9]([O:12][CH3:13])[CH2:10][NH2:11]>>[CH3:7][O:8][CH:9]([O:12][CH3:13])[CH2:10][NH:11][C:1](=[O:5])[CH:2]([CH3:4])[CH3:3]Participants
3
Procedure
The product is prepared analogously to Example 1 from isobutyryl chloride and aminoacetaldehyde dimethyl acetal. Distillation at 98° C. and 0.01 mbar gives a yield of 77%. According to GC, the product has a purity of 98%.
Workup
- distillationDistillation at 98° C.
- custom0.01 mbar gives a yield of 77%
Sources & evidence
- ORD record
- ord-649a3a20f67e409fb2c4de54c66dda1c
- Source dataset
- uspto-grants-1999_08
- Patent number
- US05932674
Reaction notes
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