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Toluene → (2S)-2-bromo-3-phenylpropanoic acid

HRID 1323
Notes
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Reaction equation

HRID 1323 reaction equation
N[C@H:2]([C:10]([OH:12])=[O:11])[CH2:3][C:4]1[CH:9]=[CH:8][CH:7]=[CH:6][CH:5]=1.[Br-:13].[K+].N([O-])=O.[Na+].C1(C)C=CC=CC=1>S(=O)(=O)(O)O.C(O)(=O)C>[Br:13][C@@H:2]([CH2:3][C:4]1[CH:9]=[CH:8][CH:7]=[CH:6][CH:5]=1)[C:10]([OH:12])=[O:11]
ParticipantsProcedureWorkupSources & evidenceReaction notes

Participants

7

Reactant 4

HCID 1140TolueneHCID 6140L-PhenylalanineHCID 253877Potassium BromideHCID 23668193Sodium Nitrite

Product 1

HCID 9816009(2S)-2-bromo-3-phenylpropanoic acid

Reagents, catalysts & solvents 2

HCID 176Acetic AcidSolvent
HCID 1118
Sulfuric Acid
Solvent

Procedure

A solution of L-phenylalanine (30.0 g., 0.175 mole) and potassium bromide (73.5 g., 0.618 mole) in 2.5N sulfuric acid (365 ml.) was cooled down to 0° (ice-salt bath) and treated portionwise with sodium nitrite (19.3 g., 0.28 mole) over a period of 1.0 hour. Stirring was continued for 1.0 hour at 0° and at room temperature for 1.0 hour after which the reaction mixture was extracted with ether (3×250 ml.). The combined organic extracts were washed with water (100 ml.) and brine (50 ml.), dried (anhydrous magnesium sulfate), filtered, evaporated to dryness and dried in vacuo to give 34.46 g., of product; Rf =0.45 (toluene:acetic acid, 95:5).

Workup

  1. extractionafter which the reaction mixture was extracted with ether (3×250 ml.)
  2. washThe combined organic extracts were washed with water (100 ml.) and brine (50 ml.)
  3. dry with materialdried (anhydrous magnesium sulfate)
  4. filtrationfiltered
  5. customevaporated to dryness
  6. customdried in vacuo
  7. customto give 34.46 g

Sources & evidence

ORD record
ord-c5d05c1fc29046a898bb31a5a6831fa6
Source dataset
uspto-grants-1998_03
DOI
10.6084/m9.figshare.5104873.v1
Patent number
US05723602

Reaction notes

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On this pageParticipantsProcedureWorkupSources & evidenceReaction notes