Reaktionsgleichung
CN.[ClH:3].[S:4]1(=[O:11])(=[O:10])[CH2:8][CH2:7][CH:6]([NH2:9])[CH2:5]1.S1(=O)(=O)CC=C[CH2:13]1>>[ClH:3].[CH3:13][NH:9][CH:6]1[CH2:7][CH2:8][S:4](=[O:11])(=[O:10])[CH2:5]1Komponenten
4
Versuchsvorschrift
The procedure of Example 1 was repeated substituting 50 percent aqueous monomethylamine (174 ml.) for the ammonium hydroxide of Example 1. Sixty-four and seven-tenths grams of a white crystalline solid was obtained for a yield of 82.2 percent of theory based upon the 2,5-dihydrothiophene 1,1-dioxide. The solid sublimes over 180° C. and melts between 205° and 210° C.
Aufarbeitung
- customSixty-four and seven-tenths grams of a white crystalline solid was obtained for a yield of 82.2 percent of theory
- customover 180° C.
- custommelts between 205° and 210° C.
Quellen und Nachweise
- ORD-Eintrag
- ord-63db3aa7dae3470fa1c0f1726e48833c
- Quelldatensatz
- uspto-grants-1983_02
- Patentnummer
- US04374040
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