Sodium Hydroxide → t-Butyl 2-(2-phenylthioethoxy)acetate

HRID 1422289Notes

Reaction equation

HRID 1422289 reaction equation
[C:1]1([S:7][CH2:8][CH2:9][OH:10])[CH:6]=[CH:5][CH:4]=[CH:3][CH:2]=1.[C:11]([O:15][C:16](=[O:19])[CH2:17]Br)([CH3:14])([CH3:13])[CH3:12].[OH-].[Na+]>[Br-].C([N+](CCCC)(CCCC)CCCC)CCC.C1(C)C=CC=CC=1>[C:1]1([S:7][CH2:8][CH2:9][O:10][CH2:17][C:16]([O:15][C:11]([CH3:14])([CH3:13])[CH3:12])=[O:19])[CH:6]=[CH:5][CH:4]=[CH:3][CH:2]=1

Participants

6

Reactant 3

HCID 14798Sodium HydroxideHCID 696852-(Phenylthio)ethanolHCID 79177tert-Butyl bromoacetate

Product 1

HCID 18779057t-Butyl 2-(2-phenylthioethoxy)acetate

Reagents, catalysts & solvents 2

HCID 74236Tetrabutylammonium BromideCatalystHCID 1140TolueneSolvent

Procedure

2-Phenylthioethanol (6.1 g), t-butylbromoacetate (7.9 ml), tetrabutylammoniumbromide (1.3 g), toluene (80 ml), and 75% aqueous sodium hydroxide (40 ml) were stirred together for 72 hours. The organic layer was separated and the aqueous layer extracted with dichloromethane. The combined organics were washed with brine, dried (MgSO4) and the solvent was removed in vacuo to provide the subtitle compound (12.07 g).

Workup

  1. customThe organic layer was separated
  2. extractionthe aqueous layer extracted with dichloromethane
  3. washThe combined organics were washed with brine
  4. dry with materialdried (MgSO4)
  5. customthe solvent was removed in vacuo

Sources & evidence

ORD record
ord-ff60fdd5033947f3ba51fb2a7824d38d
Source dataset
uspto-grants-2000_06
Patent number
US06080869

Reaction notes

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