Sodium Hydroxide → HCID 87908237, compound

HRID 1021213Notes

Reaction equation

HRID 1021213 reaction equation
C([O:4][CH2:5][C@@H:6]1[O:12][C@@H:7]1[C:8]([O:10]C)=[O:9])(=O)C.[OH-].[Na+:14]>CO.ClCCl>[Na+:14].[O:12]1[C@@H:6]([CH2:5][OH:4])[C@H:7]1[C:8]([O-:10])=[O:9]

Participants

5

Conditions

Temperature
5 °C

Procedure

A modification of the general procedure of Manchand, et. al. (Manchand, et al., 1988) is employed. A solution of methyl (2S,3S)-4-acetoxy-2,3-epoxybutanoate (81.8 g, 465 mmol) in methanol (450 mL) is cooled in an ice bath to 5° C. The solution is treated with solid sodium hydroxide at such a rate that the temperature remained less than 15° C. This mixture is stirred at 5° C. for 3 hours and diluted with dichloromethane (200 mL). The mixture is stirred at room temperature for 30 minutes. The solid is collected by filtration and washed with dichloromethane (200 mL). The resulting filter cake is dried in vacuo at room temperature to yield the title compound as a solid (58.8 g, 90% theoretical yield).

Workup

  1. customremained less than 15° C
  2. stirringThe mixture is stirred at room temperature for 30 minutes
  3. filtrationThe solid is collected by filtration
  4. washwashed with dichloromethane (200 mL)
  5. filtrationThe resulting filter cake
  6. customis dried in vacuo at room temperature

Sources & evidence

ORD record
ord-14e92a0bf6ed4c9a98227466ce629348
Source dataset
uspto-grants-2014_05
Patent number
US08716558B2

Reaction notes

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