1,3-Propanediol → Sulfamic acid, trimethylene ester
Reaction equation
S(O[CH2:6][CH2:7][O:8][S:9](=[O:12])(=[O:11])[NH2:10])(=O)(=O)N.[CH2:13]([OH:17])CCO>>[S:9]([O:17][CH2:13][CH2:6][CH2:7][O:8][S:9](=[O:11])(=[O:12])[NH2:10])(=[O:11])(=[O:8])[NH2:10]Participants
3
Procedure
1,3-Bis-O-sulfamyl-1,3-propanediol is prepared in the same manner as 1,2-bis-O-sulfamyl-1,2-ethanediol in Example 1 except that 1,3-propanediol (29.2 g., 0.385 mol.) is employed as the alkanediol.
Sources & evidence
- ORD record
- ord-25bf3b36bf064dd18771fe185b027469
- Source dataset
- uspto-grants-1977_12
- Patent number
- US04061663
Reaction notes
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