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Sulfuric Acid → 2-Bromo-4,4-dimethylpentanoic acid

HRID 1720983
Notes
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Reaction equation

HRID 1720983 reaction equation
N[C@H:2]([CH2:6][C:7]([CH3:10])([CH3:9])[CH3:8])[C:3]([OH:5])=[O:4].S(=O)(=O)(O)O.[Br-:16].[K+].N([O-])=O.[Na+]>O>[Br:16][CH:2]([CH2:6][C:7]([CH3:10])([CH3:9])[CH3:8])[C:3]([OH:5])=[O:4]
ParticipantsConditionsProcedureWorkupSources & evidenceReaction notes

Participants

6

Reactant 4

HCID 1118Sulfuric AcidHCID 253877Potassium BromideHCID 69505084-Methyl-D-leucineHCID 23668193Sodium Nitrite

Product 1

HCID 189159242-Bromo-4,4-dimethylpentanoic acid

Reagents, catalysts & solvents 1

HCID 962WaterSolvent

Conditions

Temperature
0 °C

Procedure

A solution of (R)-2-amino-4,4-dimethylpentanoic acid (950 mg, 6.55 mmol) in 2.5N aqueous sulfuric acid (13 ml, 33 mmol) was cooled to -5° C. and treated with potassium bromide (2.72 g, 22.9 mmol) in one portion. The colorless solution was treated with sodium nitrite (680 mg, 9.86 mmol) portionwise, keeping the temperature between 0° and 3° C. over a period of 25 minutes. The reaction mixture was stirred at 0° C. for one hour and at room temperature for 1.5 hours. The reaction mixture was poured into water (10 ml). The product was extracted with ether (60 ml), washed with water (20 ml) and brine (20 ml), dried (magnesium sulfate), and concentrated in vacuo to give the title product as a colorless liquid.

Workup

  1. customthe temperature between 0° and 3° C.
  2. customof 25 minutes
  3. extractionThe product was extracted with ether (60 ml)
  4. washwashed with water (20 ml) and brine (20 ml)
  5. dry with materialdried (magnesium sulfate)
  6. concentrationconcentrated in vacuo

Sources & evidence

ORD record
ord-6721c8d229ba43a59a34d2dade673432
Source dataset
uspto-grants-1996_04
DOI
10.6084/m9.figshare.5104873.v1
Patent number
US05508272

Reaction notes

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On this pageParticipantsConditionsProcedureWorkupSources & evidenceReaction notes