Nitromethane → HCID 53659307, compound
Reaction equation
[CH2:1]([O:8][C:9](=[O:16])[CH2:10][CH2:11][Si:12](Cl)([Cl:14])[Cl:13])[C:2]1[CH:7]=[CH:6][CH:5]=[CH:4][CH:3]=1.[N+:17]([CH3:20])([O-:19])=[O:18].C(N(CC)CC)C>>[CH2:1]([O:8][C:9](=[O:16])[CH2:10][CH2:11][Si:12]([Cl:14])([Cl:13])[CH2:20][N+:17]([O-:19])=[O:18])[C:2]1[CH:7]=[CH:6][CH:5]=[CH:4][CH:3]=1Participants
4
Conditions
- Temperature
- 0 °C
Procedure
298 g (1 mole) of 3-(trichlorosilyl) propionic acid benzyl ester (I) is dissolved in 540 ml (10 mol) of nitromethane and cooled to 0° C. Added dropwise 139 ml (1 mol) of triethylamine over a period of 2 hours. The mixture is then distilled through a 22 mm×4 ft. Podbielniak column packed with Heli-pak to give 3-(dichloronitromethylsilyl) propionic acid benzyl ester (II).
Workup
- distillationThe mixture is then distilled through a 22 mm×4 ft
Sources & evidence
- ORD record
- ord-39c0d085d91d4f079100a40abc95dc4d
- Source dataset
- uspto-grants-2005_09
- Patent number
- US06946272B1
Reaction notes
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