Hydrochloric Acid → HCID 131710440, compound
Reaction equation
[P:1]([CH2:5][NH:6][CH2:7][C:8]([OH:10])=[O:9])([OH:4])([OH:3])=[O:2].[ClH:11]>>[OH2:2].[ClH:11].[P:1]([CH2:5][NH:6][CH2:7][C:8]([OH:10])=[O:9])([OH:4])([OH:3])=[O:2].[P:1]([CH2:5][NH:6][CH2:7][C:8]([OH:10])=[O:9])([OH:4])([OH:3])=[O:2]Participants
3
Procedure
N-phosphonomethylglycine (10 g.) was placed in a small beaker and covered with concentrated hydrochloric acid (approximately 5 ml.). After exothermic reaction had subsided, the mixture was allowed to stand about 10 to 15 minutes. The crystalled solid was washed with tetrahydrofuran and then air-dried to yield an essentially quantitative yield of N-phosphonomethylglycine hemihydrochloride hemihydrate (m.p. greater than 300° C.).
Workup
- customAfter exothermic reaction
- washThe crystalled solid was washed with tetrahydrofuran
- customair-dried
Sources & evidence
- ORD record
- ord-a81676a4b4574306bc73b2652edfcb3e
- Source dataset
- uspto-grants-1983_09
- Patent number
- US04405531
Reaction notes
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