Lithium Hydroxide → 2-Carboxy-2-(t-butyl)thiomethyl-indan

HRID 1451242Notes

Reaction equation

HRID 1451242 reaction equation
[C:1]([C:5]1([CH2:14][S:15][C:16]([CH3:19])([CH3:18])[CH3:17])[CH2:13][C:12]2[C:7](=[CH:8][CH:9]=[CH:10][CH:11]=2)[CH2:6]1)([O:3]C)=[O:2].[OH-].[Li+]>CO>[C:1]([C:5]1([CH2:14][S:15][C:16]([CH3:19])([CH3:18])[CH3:17])[CH2:13][C:12]2[C:7](=[CH:8][CH:9]=[CH:10][CH:11]=2)[CH2:6]1)([OH:3])=[O:2]

Participants

4

Reactant 2

HCID 3939Lithium HydroxideHCID 158143772-Carbomethoxy-2-(t-butyl)thiomethyl-indan

Product 1

HCID 158143782-Carboxy-2-(t-butyl)thiomethyl-indanYield 96%

Reagents, catalysts & solvents 1

HCID 887MethanolSolvent

Procedure

Dissolve 2-carbomethoxy-2-(t-butyl)thiomethyl-indan (557 mg, 2.0 mmol) in methanol (15 mL) and add 1N lithium hydroxide (3.5 mL). Warm briefly to effect solution then stir at room temperature under an argon atmosphere for 1 hour. Reflux for 6 hours, concentrate in vacuo to a volume of 3 mL and dilute to a volume of 15 mL with water. Wash with methylene chloride and acidify and aqueous phase with excess 2N hydrochloric acid. After 5 minutes, collect the resulting white precipitate by filtration and dry to give 2-carboxy-2-(t-butyl)thiomethyl-indan (506 mg, 96%); mp 158°-163° C.

Workup

  1. temperatureWarm briefly
  2. temperatureReflux for 6 hours
  3. concentrationconcentrate in vacuo to a volume of 3 mL
  4. additiondilute to a volume of 15 mL with water
  5. washWash with methylene chloride
  6. waitAfter 5 minutes
  7. customcollect the resulting white precipitate
  8. filtrationby filtration
  9. customdry

Sources & evidence

ORD record
ord-be75bd7a12c940d5a5e234d27fb11b00
Source dataset
uspto-grants-1997_02
Patent number
US05604221

Reaction notes

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