tert-Butyl methyl ether → HCID 9793812, compound

HRID 1064439Notes

Reaction equation

HRID 1064439 reaction equation
[CH:1]([CH:4]([CH:8]([CH3:10])[CH3:9])[C:5]([NH2:7])=[O:6])([CH3:3])C.[CH3:11]OC(C)(C)C>>[CH2:1]([C@@H:4]([CH:8]([CH3:9])[CH3:10])[C:5]([NH2:7])=[O:6])[CH2:3][CH3:11]

Participants

3

Procedure

Assay of plasma samples: to test tubes containing 2 μg of the internal standard (diisopropyl acetamide), 0.5 ml of plasma (thawed at room temperature) and 5 ml of tert-butyl methyl ether (TBME) was added. The test tubes were vigorously vortexed for 30 sec and centrifuged at 3000 g for 10 minutes. The organic phase was separated and dried under reduced pressure using a vortex evaporator. Samples were then reconstituted with 150 μl of chloroform and dried under reduced pressure without vortexing. The sample was again reconstituted with 30 μl of chloroform, of which 2 μl were injected into the GC apparatus.

Workup

  1. additionwas added
  2. waitcentrifuged at 3000 g for 10 minutes
  3. customThe organic phase was separated
  4. customdried under reduced pressure
  5. customa vortex evaporator
  6. customdried under reduced pressure without vortexing

Sources & evidence

ORD record
ord-19039cf30e564ed1a92aacb0a5922940
Source dataset
uspto-grants-2005_11
Patent number
US06969732B2

Reaction notes

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