Thionyl Chloride → HCID 11268015, compound
Reaction equation
S(Cl)([Cl:3])=O.[Cl:5][Ge:6]([Cl:19])([Cl:18])[CH:7]([C:12]1[CH:17]=[CH:16][CH:15]=[CH:14][CH:13]=1)[CH2:8][C:9](O)=[O:10]>>[Cl:5][Ge:6]([Cl:19])([Cl:18])[CH:7]([C:12]1[CH:17]=[CH:16][CH:15]=[CH:14][CH:13]=1)[CH2:8][C:9]([Cl:3])=[O:10]Participants
3
Procedure
Sixty grams of thionyl chloride was added to 16.4 g (0.05 mol) of β-(trichlorogermyl)hydrocinnamic acid (7), and the mixture was heated under reflux for 2 hours. Then excess thionyl chloride was distilled away in the usual manner. The residue, upon vacuum distillation, gave 12.9 g of a fraction, bp 148°-149° C./4 mmHg. The yield was 69.1%.
Workup
- temperaturethe mixture was heated
- temperatureunder reflux for 2 hours
- distillationThen excess thionyl chloride was distilled away in the usual manner
- distillationThe residue, upon vacuum distillation
- customgave 12.9 g of a fraction, bp 148°-149° C./4 mmHg
Sources & evidence
- ORD record
- ord-2b4e152379aa46ec9ead4b63a5b316df
- Source dataset
- uspto-grants-1986_04
- Patent number
- US04579961
Reaction notes
Loading…