Nitromethane → HCID 53659307, compound

HRID 618435Notes

Reaction equation

HRID 618435 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]=1

Participants

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

  1. distillationThe mixture is then distilled through a 22 mm×4 ft

Sources & evidence

ORD record
ord-ed1ad7d686f24882bcbd34b19102e900
Source dataset
uspto-grants-1999_09
Patent number
US05952462

Reaction notes

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