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Aluminum hydroxide (Al(OH)3), hydrate → Aluminum tris(2-(5,5-dimethyl-2-oxido-1,3,2-dioxaphosphinan-2yl)acetate)

HRID 531405
Notes
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Reaction equation

HRID 531405 reaction equation
[CH3:1][C:2]1([CH3:13])[CH2:7][O:6][P:5]([CH2:9][C:10]([OH:12])=[O:11])(=[O:8])[O:4][CH2:3]1.O.[OH-].[Al+3:16].[OH-].[OH-]>O>[CH3:1][C:2]1([CH3:13])[CH2:7][O:6][P:5]([CH2:9][C:10]([O-:12])=[O:11])(=[O:8])[O:4][CH2:3]1.[CH3:1][C:2]1([CH3:13])[CH2:7][O:6][P:5]([CH2:9][C:10]([O-:12])=[O:11])(=[O:8])[O:4][CH2:3]1.[CH3:1][C:2]1([CH3:13])[CH2:7][O:6][P:5]([CH2:9][C:10]([O-:12])=[O:11])(=[O:8])[O:4][CH2:3]1.[Al+3:16]
ParticipantsConditionsProcedureWorkupSources & evidenceReaction notes

Participants

4

Reactant 2

HCID 22721319Aluminum hydroxide (Al(OH)3), hydrateHCID 901017352-(5,5-Dimethyl-2-oxido-1,3,2-dioxaphosphinan-2-yl)acetic acid

Product 1

HCID 131735658Aluminum tris(2-(5,5-dimethyl-2-oxido-1,3,2-dioxaphosphinan-2yl)acetate)

Reagents, catalysts & solvents 1

HCID 962WaterSolvent

Conditions

Temperature
90 °C

Procedure

Prepare a reaction vessel from a 1000 mL single neck round bottom flask by fitting with a condenser with a nitrogen inlet. Charge the vessel with 31.55 g 2-(5,5-dimethyl-2-oxido-1,3,2-dioxaphosphinan-2-yl)acetic acid followed by 100 mL water and 4.38 g aluminum hydroxide monohydrate. Heat the resulting solution to 90° C. and hold at that temperature for 24 hours. Isolate the solid by vacuum filtration using a fritted funnel and wash with 400 mL acetone. Transfer the solid product to a glass bottle and place in a vacuum oven to dry overnight. The yield of the solid product of Aluminum tris(2-(5,5-dimethyl-2-oxido-1,3,2-dioxaphosphinan-2yl)acetate) is 31.25 g.

Workup

  1. customPrepare a reaction vessel from a 1000 mL single neck round bottom flask
  2. customby fitting with a condenser with a nitrogen inlet
  3. customIsolate the solid
  4. filtrationby vacuum filtration
  5. washwash with 400 mL acetone
  6. customto dry overnight

Sources & evidence

ORD record
ord-f55d4103f4c54a7f9b0da8b7a7383306
Source dataset
uspto-grants-2016_05
DOI
10.6084/m9.figshare.5104873.v1
Patent number
US09353246B2

Reaction notes

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On this pageParticipantsConditionsProcedureWorkupSources & evidenceReaction notes