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Hydrochloric Acid → H-Leu-Ser-OCH3.HCl

HRID 1632418
Notes
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Reaction equation

HRID 1632418 reaction equation
[NH:1](C(OCC1C=CC=CC=1)=O)[C@H:2]([C:7]([NH:9][C@H:10]([C:13]([O:15][CH3:16])=[O:14])[CH2:11][OH:12])=[O:8])[CH2:3][CH:4]([CH3:6])[CH3:5].[ClH:27].[H][H]>[Pd]>[NH2:1][C@H:2]([C:7]([NH:9][C@H:10]([C:13]([O:15][CH3:16])=[O:14])[CH2:11][OH:12])=[O:8])[CH2:3][CH:4]([CH3:5])[CH3:6].[ClH:27]
ParticipantsProcedureWorkupSources & evidenceReaction notes

Participants

5

Reactant 3

HCID 313Hydrochloric AcidHCID 7350008Z-Leu-ser-omeHCID 178418361HCID 178418361, compound

Product 1

HCID 13875640H-Leu-Ser-OCH3.HCl

Reagents, catalysts & solvents 1

HCID 23938PalladiumCatalyst

Procedure

4.20 Grams of Z-Leu-Ser-OCH3 was suspended in a mixture of 40 ml of methan-1 with 11.46 ml of 1N-hydrochloric acid, then a small amount of palladium black was added to the suspension, stirred for 18 hours under the condition of introducing hydrogen gas. After completion of the reaction the catalyst was removed by suction filtration, the filtrate was subjected to distillation under a reduced pressure, further to the residue obtained was added water and distillation under a reduced pressure were repeated 3 times. The residue thus obtained was dried under a reduced pressure in a desiccator containing phosphorus pentoxide as the desiccant to obtain the desired product.

Workup

  1. customAfter completion of the reaction the catalyst
  2. customwas removed by suction filtration
  3. distillationthe filtrate was subjected to distillation under a reduced pressure, further to the residue
  4. customobtained
  5. additionwas added
  6. distillationwater and distillation under a reduced pressure
  7. customThe residue thus obtained
  8. customwas dried under a reduced pressure in a desiccator
  9. additioncontaining phosphorus pentoxide as the desiccant

Sources & evidence

ORD record
ord-d1b8e43d63f2444392ef782bc01839fe
Source dataset
uspto-grants-1984_10
DOI
10.6084/m9.figshare.5104873.v1
Patent number
US04474754

Reaction notes

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