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1(3H)-Isobenzofuranone, 3-hydroxy-7-methoxy- → HCID 16748834, compound

HRID 22172
Notes
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Reaction equation

HRID 22172 reaction equation
[OH:1][CH:2]1[C:11]2[C:6](=[C:7]([O:12]C)[CH:8]=[CH:9][CH:10]=2)[C:4](=[O:5])[O:3]1.[Cl-].[Cl-].[Cl-].[Al+3]>C(Cl)Cl>[OH:1][CH:2]1[C:11]2[C:6](=[C:7]([OH:12])[CH:8]=[CH:9][CH:10]=2)[C:4](=[O:5])[O:3]1
ParticipantsConditionsProcedureWorkupSources & evidenceReaction notes

Participants

4

Reactant 2

HCID 27525831(3H)-Isobenzofuranone, 3-hydroxy-7-methoxy-HCID 6451240Aluminum(III) Chloride

Product 1

HCID 16748834HCID 16748834, compound

Reagents, catalysts & solvents 1

HCID 6344DichloromethaneSolvent

Conditions

Temperature
27 °C

Procedure

3.0 g of 3-hydroxy-7-methoxy-phthalide ]see B. L. Chenard et al., J. Org. Chem. 49, 318 (1984)] are introduced in portions into a suspension of 8.2 g of aluminium trichloride in 50 ml of methylene chloride, the internal temperature being maintained at 27° C. The mixture is stirred at room temperature for a further 5 hours, is then poured into 200 ml of ice-cold 1N hydrochloric acid and extracted three times with 200 ml of ethyl acetate each time. The organic solution is washed with sodium chloride solution and dried over anhydrous magnesium sulfate. Evaporation of the solvent and recrystallisation from ethyl acetate and n-hexane yield pure 3,7-dihydroxyphthalide, m.p. 124°-126° C.

Workup

  1. extractionextracted three times with 200 ml of ethyl acetate each time
  2. washThe organic solution is washed with sodium chloride solution
  3. dry with materialdried over anhydrous magnesium sulfate
  4. customEvaporation of the solvent and recrystallisation from ethyl acetate and n-hexane

Sources & evidence

ORD record
ord-2eb9932e21774af2b0a27f1f00230fb5
Source dataset
uspto-grants-1995_06
DOI
10.6084/m9.figshare.5104873.v1
Patent number
US05428002

Reaction notes

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On this pageParticipantsConditionsProcedureWorkupSources & evidenceReaction notes