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Hydrochloric Acid → HCID 14503313, compound

HRID 442647
Notes
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Reaction equation

HRID 442647 reaction equation
C(OC([NH:11][C@@H:12]([CH:20]([CH3:22])[CH3:21])C(OC(=O)C)C#N)=O)C1C=CC=CC=1.Cl.C1([O:30]C)C=CC=CC=1.[O:32]1[CH2:37][CH2:36][O:35]CC1>>[NH2:11][C@@H:12]([CH:20]([CH3:22])[CH3:21])[CH:36]([OH:35])[C:37]([OH:32])=[O:30]
ParticipantsProcedureWorkupSources & evidenceReaction notes

Participants

5

Reactant 4

HCID 313Hydrochloric AcidHCID 7519AnisoleHCID 312751,4-DioxaneHCID 228716173-(S)-[(benzyloxycarbonyl)amino]-2-acetoxy-4-methylpentanenitrile

Product 1

HCID 14503313HCID 14503313, compoundYield 75%

Procedure

To a solution containing 3-(S)-[(benzyloxycarbonyl)amino]-2-acetoxy-4-methylpentanenitrile (see example 1 of WO 96/16080) (15.2 g, 50.0 mmol) in 183 mL of dioxane was added 183 mL of concentrated hydrochloric acid and 7.45 mL of anisole. The reaction mixture was heated to reflux overnight. The hydrolysis reaction was allowed to cool to room temperature and then concentrated in vacuo. The resulting aqueous solution was extracted with ether (2×). The aqueous phase was placed on a Dowex 50X8-100 column (H+ form, preeluted with deionized water to pH=7). The column was eluted with 2.0N ammonium hydroxide and the pure fractions concentrated to afford 5.53 g (75%) of 3-(S)-amino-2-(R,S)-hydroxy-4-methylpentanoic acid as a pale yellow solid. FAB MS [M+H] m/z; Calcd: 148, Found: 148.

Workup

  1. temperatureThe reaction mixture was heated
  2. temperatureto reflux overnight
  3. customThe hydrolysis reaction
  4. concentrationconcentrated in vacuo
  5. extractionThe resulting aqueous solution was extracted with ether (2×)
  6. washThe column was eluted with 2.0N ammonium hydroxide
  7. concentrationthe pure fractions concentrated

Sources & evidence

ORD record
ord-5067021c4e92440ca789805a09afaf3b
Source dataset
uspto-grants-1999_04
DOI
10.6084/m9.figshare.5104873.v1
Patent number
US05891852

Reaction notes

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On this pageParticipantsProcedureWorkupSources & evidenceReaction notes