Sodium Sulfite → HCID 59456523, compound

HRID 1922621Notes

Reaction equation

HRID 1922621 reaction equation
[CH:1](=[C:3]1/[CH2:4][CH2:5][C@@H:6]2[C@:11]/1([CH3:12])[CH2:10][CH2:9][CH2:8][C@@H:7]2[OH:13])\[CH3:2].ClC1C=CC=C(C(OO)=[O:22])C=1.C(=O)([O-])O.[Na+].S([O-])([O-])=O.[Na+].[Na+]>C(OCC)(=O)C.CCCCCCC>[CH3:2][C@@H:1]1[O:22][C@@:3]21[C@:11]1([CH3:12])[C@H:6]([C@@H:7]([OH:13])[CH2:8][CH2:9][CH2:10]1)[CH2:5][CH2:4]2

Participants

7

Conditions

Temperature
4.400000095367432 °C

Procedure

(Z,3aR,4S,7aS)-1-ethylidene-octahydro-7a-methyl-1H-indene-4-ol (Compound 6: 663.1 mg, 3.18 mmol) synthesized in accordance with the method described in J. Org. Chem. 2001, 66, 626-628 was dissolved in ethyl acetate (3.1 ml), and the solution was cooled to 4.4° C. Meta-chloroperbenzoic acid (913 mg, 3.44 mmol) was added to the reaction solution over 9 minutes. After stirring the reaction solution at 2° C. for 1 hour, aqueous sodium hydrogen carbonate solution (2 ml) and aqueous sodium sulfite solution (1 ml) were added thereto, and the mixed solution was stirred and separated. The obtained organic layer was washed with aqueous sodium hydrogen carbonate solution (2 ml) and dried over magnesium sulfate, and then the solvent was evaporated under reduced pressure. To the obtained reaction mixture, seed crystals were added, and heptane (1.8 ml) was added thereto, followed by collecting the precipitated crystals by filtration to obtain (1R,3aR,4S,7aS,3′S)-3′,7a-dimethyl-4-hydroxyoctahydrospiro(indene-1,2′-oxirane) (382.8 mg, 61%).

Workup

  1. stirringthe mixed solution was stirred
  2. customseparated
  3. washThe obtained organic layer was washed with aqueous sodium hydrogen carbonate solution (2 ml)
  4. dry with materialdried over magnesium sulfate
  5. customthe solvent was evaporated under reduced pressure
  6. customTo the obtained reaction mixture, seed crystals
  7. additionwere added
  8. customby collecting the precipitated crystals
  9. filtrationby filtration

Sources & evidence

ORD record
ord-956b2f4a0a904814a26b469a3420dae5
Source dataset
uspto-grants-2012_05
Patent number
US08173824B2

Reaction notes

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