Phosphorus pentachloride → HCID 178479351, compound
Reaction equation
[ClH:1].[C:2]([NH:10][CH2:11][C:12]([OH:14])=O)(=[NH:9])[C:3]1[CH:8]=[CH:7][CH:6]=[CH:5][CH:4]=1.P(Cl)(Cl)(Cl)(Cl)[Cl:16]>C(Cl)Cl>[ClH:16].[C:2]([NH:10][CH2:11][C:12]([Cl:1])=[O:14])(=[NH:9])[C:3]1[CH:8]=[CH:7][CH:6]=[CH:5][CH:4]=1Participants
4
Reactant 2
Product 1
Reagents, catalysts & solvents 1
Procedure
To benzimidoylaminoacetic acid hydrochloride (2.2 g., 10 mmoles) in 40 ml. of dry methylene chloride is added 2.5 g. (12 mmoles) of phosphorous pentachloride, and the reaction mixture allowed to stir overnight at room temperature. The product is filtered, washed successively with methylene chloride (50 ml. ), chloroform 2× 75 ml.) and hexane (50 ml.) and dried in vacuo, 2.5 g. (99% yield).
Workup
- filtrationThe product is filtered
- washwashed successively with methylene chloride (50 ml. ), chloroform 2× 75 ml
- dry with material) and hexane (50 ml.) and dried in vacuo, 2.5 g
Sources & evidence
- ORD record
- ord-8472ed6ac61a4e67b131e5ed0c83f3cf
- Source dataset
- uspto-grants-1977_05
- Patent number
- US04025506
Reaction notes
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