Ammonium Chloride → HCID 15476078, compound

HRID 2289366Notes

Reaction equation

HRID 2289366 reaction equation
[C:1]1([CH3:15])[CH:6]=[CH:5][C:4]([S:7]([O:10][CH2:11][C@@H:12]2[O:14][CH2:13]2)(=[O:9])=[O:8])=[CH:3][CH:2]=1.[Cl-].[NH4+]>C1COCC1.[Cu](Cl)(Cl)(Cl)Cl.[Li]>[C:1]1([CH3:15])[CH:6]=[CH:5][C:4]([S:7]([O:10][CH2:11][C@H:12]([OH:14])[CH2:13][CH2:6][C@@H:1]([CH3:15])[CH2:2][CH3:3])(=[O:9])=[O:8])=[CH:3][CH:2]=1

Participants

5

Conditions

Temperature
-50 °C

Procedure

In a 500 ml flask was put 18 ml of a 0.1 ML-1 solution of lithium copper tetrachloride in dried THF, followed by cooling to -50° C. The above prepared Grignard reagent was added thereto over 5 minutes, and the mixture was reacted at that temperature for 20 minutes. To the reaction mixture was added dropwise a solution of 8.07 g of (R)-glycidyl p-toluenesulfonate (produced by Aldrich Chemical Co., Inc.) in 70 ml of dried THF at the same temperature over 20 minutes through a dropping funnel, followed by further reacting for 1.5 hours. The resulting reaction mixture was poured into a saturated ammonium chloride aqueous solution and extracted with diethyl ether. The extract was washed twice with a saturated sodium chloride aqueous solution, and the solvent was removed by distillation under reduced pressure to obtain 10.1 g (95%) of a crude product.

Workup

  1. customIn a 500 ml flask was put
  2. additionwas added
  3. customthe mixture was reacted at that temperature for 20 minutes
  4. waitby further reacting for 1.5 hours
  5. customThe resulting reaction mixture
  6. extractionextracted with diethyl ether
  7. washThe extract was washed twice with a saturated sodium chloride aqueous solution
  8. customthe solvent was removed by distillation under reduced pressure

Sources & evidence

ORD record
ord-c10098b343d0402f9838b38aa281f156
Source dataset
uspto-grants-2000_07
Patent number
US06093345

Reaction notes

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