1-Benzhydrylaminoheptanephosphonous acid → 1-Amino-n-heptanephosphonous acid
Reaction equation
C([NH:14][CH:15]([P:22]([OH:24])[OH:23])[CH2:16][CH2:17][CH2:18][CH2:19][CH2:20][CH3:21])(C1C=CC=CC=1)C1C=CC=CC=1.C(NC(P(O)O)C(C)C)(C1C=CC=CC=1)C1C=CC=CC=1>>[NH2:14][CH:15]([P:22]([OH:24])[OH:23])[CH2:16][CH2:17][CH2:18][CH2:19][CH2:20][CH3:21]Participants
3
Procedure
The procedure described in Example 1C was repeated using DL-1-benzhydrylaminoheptanephosphonous acid as starting material instead of DL-1-benzhydrylamino-2-methylpropanephosphonous acid to give DL-1-amino-n-heptanephosphonous acid of melting point 208°-210° (dec.).
Sources & evidence
- ORD record
- ord-f8df823400f746a5bd97e3f43ac869f0
- Source dataset
- uspto-grants-1979_04
- Patent number
- US04147780
Reaction notes
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