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Sodium Hydroxide → O-methoxymethyl-N-methyl-N-(2-nitrophenylthio)-beta-hydroxytyrosine

HRID 1587284
Notes
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Reaction equation

HRID 1587284 reaction equation
[CH3:1][O:2][CH2:3][O:4][C:5]1[CH:18]=[CH:17][C:8]([CH:9]([OH:16])[C@@H:10]([C:13]([OH:15])=[O:14])[NH:11][CH3:12])=[CH:7][CH:6]=1.C[Si](C([Si](C)(C)C)C(N)=O)(C)C.[N+:31]([C:34]1[CH:39]=[CH:38][CH:37]=[CH:36][C:35]=1[S:40]Cl)([O-:33])=[O:32].[OH-].[Na+]>ClCCl>[CH3:1][O:2][CH2:3][O:4][C:5]1[CH:6]=[CH:7][C:8]([CH:9]([OH:16])[C@@H:10]([C:13]([OH:15])=[O:14])[N:11]([CH3:12])[S:40][C:35]2[CH:36]=[CH:37][CH:38]=[CH:39][C:34]=2[N+:31]([O-:33])=[O:32])=[CH:17][CH:18]=1
ParticipantsConditionsProcedureWorkupSources & evidenceReaction notes

Participants

6

Reactant 4

HCID 14798Sodium HydroxideHCID 243192-Nitrobenzenesulfenyl chloride2×HCID 11708267Bistrimethylsilylacetamid2×HCID 53901170O-methoxymethyl-N-methyl-beta-hydroxytyrosine

Product 1

HCID 54196694O-methoxymethyl-N-methyl-N-(2-nitrophenylthio)-beta-hydroxytyrosineYield 85%

Reagents, catalysts & solvents 1

HCID 6344DichloromethaneSolvent2×

Conditions

Temperature
0 °C

Procedure

To a solution of O-methoxymethyl-N-methyl-β-hydroxytyrosine (15.1 g) and bis(trimethylsilyl)acetamide (25 ml) in dichloromethane (150 ml) was added a solution of 2-nitrophenylsulfenyl chloride (11.2 g) in dichloromethane (50 ml). After stirring for 2 hours at 0° C., bis(trimethylsilyl)acetamide (10 ml) and 2-nitrophenylsulfenyl chloride (5.6 g) was added to the solution. The mixture was stirred for 3 hours at room temperature and added to 1N-sodium hydroxide (200 ml). The organic layer was washed with water (300 ml) and the aqueous solutions were combined. After the aqueous solution was acidified with diluted hydrochloric acid, the product was extracted with ethyl acetate (300 ml) and the extract was washed with water (100 ml×3). After the solution was dried over magnesium sulfate, the solvent was removed in vacuo to give O-methoxymethyl-N-methyl-N-(2-nitrophenylthio)-β-hydroxytyrosine (20.5 g).

Workup

  1. stirringThe mixture was stirred for 3 hours at room temperature
  2. washThe organic layer was washed with water (300 ml)
  3. extractionthe product was extracted with ethyl acetate (300 ml)
  4. washthe extract was washed with water (100 ml×3)
  5. dry with materialAfter the solution was dried over magnesium sulfate
  6. customthe solvent was removed in vacuo

Sources & evidence

ORD record
ord-51a3820cfad94e8ba290507c4c7ed349
Source dataset
uspto-grants-1993_06
DOI
10.6084/m9.figshare.5104873.v1
Patent number
US05217952

Reaction notes

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On this pageParticipantsConditionsProcedureWorkupSources & evidenceReaction notes