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Ethyl 3-bromopropionate → 4-Cyano-4-(3,4-dichlorophenyl)-7-(tetrahydropyran-4-yloxy)-heptanoic Acid Ethyl Ester

HRID 1637183
Notes
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Reaction equation

HRID 1637183 reaction equation
C[Si](C)(C)[N-][Si](C)(C)C.[K+].[Cl:11][C:12]1[CH:13]=[C:14]([CH:19]([CH2:22][CH2:23][CH2:24][O:25][CH:26]2[CH2:31][CH2:30][O:29][CH2:28][CH2:27]2)[C:20]#[N:21])[CH:15]=[CH:16][C:17]=1[Cl:18].Br[CH2:33][CH2:34][C:35]([O:37][CH2:38][CH3:39])=[O:36]>C1COCC1>[CH2:38]([O:37][C:35](=[O:36])[CH2:34][CH2:33][C:19]([C:20]#[N:21])([C:14]1[CH:15]=[CH:16][C:17]([Cl:18])=[C:12]([Cl:11])[CH:13]=1)[CH2:22][CH2:23][CH2:24][O:25][CH:26]1[CH2:31][CH2:30][O:29][CH2:28][CH2:27]1)[CH3:39]
ParticipantsProcedureWorkupSources & evidenceReaction notes

Participants

5

Reactant 3

HCID 68320Ethyl 3-bromopropionateHCID 3251421Potassium bis(trimethylsilyl)amideHCID 158876512-(3,4-Dichloro-phenyl)-5-(tetrahydro-pyran-4-yloxy)-pentanenitrile

Product 1

HCID 158876524-Cyano-4-(3,4-dichlorophenyl)-7-(tetrahydropyran-4-yloxy)-heptanoic Acid Ethyl EsterYield 94.4%

Reagents, catalysts & solvents 1

HCID 8028
Tetrahydrofuran
Solvent
2×

Procedure

Potassium hexamethyldisilazide (0.5 M in toluene, 285 mL, 0.143 mol) was added dropwise to a solution of (4) (39 g, 0.119 mol) in THF (240 mL) under nitrogen and stirred at room temperature for 1 hour. A solution of ethyl 3-bromopropionate (22.8 mL, 0.178 mol, 1.5 eq) in THF (45 mL) was added to the reaction mixture all at once. After stirring at room temperature for 4 hours, the reaction was quenched with saturated NH4Cl solution (20 mL). The organic solution was dried over MgSO4, and solvent is evaporated. The crude oil was purified by flashed chromatography (hexane-AcOEt/8:1) to give light yellow oil (48.03 g, 94.4% yield).

Workup

  1. stirringAfter stirring at room temperature for 4 hours
  2. customthe reaction was quenched with saturated NH4Cl solution (20 mL)
  3. dry with materialThe organic solution was dried over MgSO4, and solvent
  4. customis evaporated
  5. customThe crude oil was purified

Sources & evidence

ORD record
ord-e92dca56205a400289b8dfb2a53a941f
Source dataset
uspto-grants-2000_03
DOI
10.6084/m9.figshare.5104873.v1
Patent number
US06040316

Reaction notes

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On this pageParticipantsProcedureWorkupSources & evidenceReaction notes