Thiophosgene → HCID 85844959, compound
Reaction equation
Cl.[NH2:2][C:3]1[CH:8]=[C:7]([P:9]([OH:12])(=[O:11])[OH:10])[CH:6]=[C:5]([P:13]([OH:16])(=[O:15])[OH:14])[CH:4]=1.[C:17](Cl)(Cl)=[S:18]>O>[N:2]([C:3]1[CH:8]=[C:7]([P:9]([OH:10])(=[O:12])[OH:11])[CH:6]=[C:5]([P:13]([OH:16])(=[O:14])[OH:15])[CH:4]=1)=[C:17]=[S:18]Participants
4
Reactant 2
Product 1
Reagents, catalysts & solvents 1
Conditions
- Temperature
- 20 °C
Procedure
Aniline-3,5-diphosphonic acid hydrochloride(500 mg, 1.73 mmole) was dissolved in water(5 ml) and thiophosgene(600 mg, 5.2 mmole) was added and the mixture stirred vigorously at 20° C. for 2.5 hours. Volatiles were removed in vacuo and the residue was dissolved in water(10 ml), filtered and lyophilised. 490 mg. 96%
Workup
- customVolatiles were removed in vacuo
- dissolutionthe residue was dissolved in water(10 ml)
- filtrationfiltered
Sources & evidence
- ORD record
- ord-77256170543f47ff8d01a7322d66476b
- Source dataset
- uspto-grants-2009_08
- Patent number
- US07572459B2
Reaction notes
Loading…