HCID 21432960, compound → HCID 21432958, compound
Reaction equation
[C:1]([CH2:3][CH2:4][O:5][P:6]([CH2:9][NH:10][CH2:11][C:12]([O:14]CC)=[O:13])([OH:8])=[O:7])#[N:2]>O>[C:1]([CH2:3][CH2:4][O:5][P:6]([CH2:9][NH:10][CH2:11][C:12]([OH:14])=[O:13])([OH:8])=[O:7])#[N:2]Participants
3
Reactant 1
Product 1
Reagents, catalysts & solvents 1
Procedure
25 g (0.1 mols) of ethyl N-[O-(β-cyanoethyl)-phosphonomethyl]-aminoacetate in 200 ml of water are heated under reflux for 16 hours. The water is then evaporated off in vacuo in a rotary evaporator and the residue is dried at 50° under high vacuum. Thereafter the residue is warmed with 300 ml of ethanol.
Workup
- temperatureunder reflux for 16 hours
- customThe water is then evaporated off in vacuo in a rotary evaporator
- customthe residue is dried at 50° under high vacuum
- temperatureThereafter the residue is warmed with 300 ml of ethanol
Sources & evidence
- ORD record
- ord-95113e0a13cc4c06b23ccbdf92051cb6
- Source dataset
- uspto-grants-1977_05
- Patent number
- US04025331
Reaction notes
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