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Potassium Bromide → (S)-2-bromo-4-methylpentanoic acid

HRID 1331
Notes
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Reaction equation

HRID 1331 reaction equation
[Br-:1].[K+].N[C@@H:4]([C:9]([OH:11])=[O:10])[CH2:5][CH:6]([CH3:8])[CH3:7].N([O-])=O.[Na+]>S(=O)(=O)(O)O>[Br:1][C@@H:4]([CH2:5][CH:6]([CH3:8])[CH3:7])[C:9]([OH:11])=[O:10]
ParticipantsConditionsProcedureWorkupSources & evidenceReaction notes

Participants

5

Reactant 3

HCID 253877Potassium BromideHCID 439524D-LeucineHCID 23668193Sodium Nitrite

Product 1

HCID 12697061(S)-2-bromo-4-methylpentanoic acid

Reagents, catalysts & solvents 1

HCID 1118Sulfuric AcidSolvent

Conditions

Temperature
-10 °C

Procedure

Potassium bromide (9.5 g., 80 mmol.) was added to a stirred solution of D-leucine (3.0 g., 23 mmol.) in 2.5N sulfuric acid (47 ml.) at room temperature. The reaction mixture was cooled to -10° C. and solid sodium nitrite (2.4 g., 34 mmol.) was added portionwise, maintaining the temperature between -10° and -5° C. After addition was complete, the reaction was stirred for 1 hour and then warmed to room temperature and stirred for another hour. The reaction mixture was then extracted twice with ether, the ether extracts were washed once with water, dried (magnesium sulfate), filtered and evaporated to give 2.7 g. of crude title product.

Workup

  1. temperaturemaintaining the temperature between -10° and -5° C
  2. additionAfter addition
  3. temperaturewarmed to room temperature
  4. stirringstirred for another hour
  5. extractionThe reaction mixture was then extracted twice with ether
  6. washthe ether extracts were washed once with water
  7. dry with materialdried (magnesium sulfate)
  8. filtrationfiltered
  9. customevaporated
  10. customto give 2.7 g

Sources & evidence

ORD record
ord-f8e6f6d403494c7b94171529ebac16f6
Source dataset
uspto-grants-1998_03
DOI
10.6084/m9.figshare.5104873.v1
Patent number
US05723602

Reaction notes

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On this pageParticipantsConditionsProcedureWorkupSources & evidenceReaction notes