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Dimethylformamide → (S)-3-[(S)-1-(3-Chloro-2-methylphenoxy)but-3-enyl]-pyrrolidine

HRID 1671392
Notes
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Reaction equation

HRID 1671392 reaction equation
C(OC([N:8]1[CH2:12][CH2:11][C@H:10]([C@@H:13]([OH:17])[CH2:14][CH:15]=[CH2:16])[CH2:9]1)=O)(C)(C)C.CN(C=O)C.[H-].[Na+].[Cl:25][C:26]1[CH:31]=[CH:30][CH:29]=[C:28](F)[C:27]=1[CH3:33]>>[Cl:25][C:26]1[C:27]([CH3:33])=[C:28]([CH:29]=[CH:30][CH:31]=1)[O:17][C@H:13]([C@H:10]1[CH2:11][CH2:12][NH:8][CH2:9]1)[CH2:14][CH:15]=[CH2:16]
ParticipantsConditionsProcedureWorkupSources & evidenceReaction notes

Participants

5

Reactant 4

HCID 6228DimethylformamideHCID 99332-Chloro-6-fluorotolueneHCID 24758Sodium hydride2×HCID 58104609(S)-3-((S)-1-hydroxy-but-3-enyl)pyrrolidine-1-carboxylic acid t-butyl ester

Product 1

HCID 58104608(S)-3-[(S)-1-(3-Chloro-2-methylphenoxy)but-3-enyl]-pyrrolidine

Conditions

Temperature
70 °C

Procedure

(S)-3-((S)-1-Hydroxy-but-3-enyl)pyrrolidine-1-carboxylic acid t-butyl ester (31 mg, 130 μmmol) was dissolved in DMF (470 μL, 6.1 mmol). 60% Sodium hydride in oil (0.4:0.6, sodium hydride:mineral oil, 10.1 mg, 169 μmmol) was carefully added, and the mixture allowed to stand for 15 minutes. 2-Chloro-6-fluorotoluene (47.0 μL, 390 μmmol) was added. The mixture was stirred at 70° C. for 3 hours. The reaction was quenched with MeOH, and the solvent was removed. 1.2M HCl in EtOH (630 μL, 760 μmmol) was added, and the mixture was stirred overnight. The product was concentrated and purified by preparative HPLC to yield the title compound as a mono-TFA salt (1 mg, 100% purity). MS m/z: [M+H]+ calcd for C15H20ClNO, 266.12; found 266.0.

Workup

  1. customThe reaction was quenched with MeOH
  2. customthe solvent was removed
  3. addition1.2M HCl in EtOH (630 μL, 760 μmmol) was added
  4. stirringthe mixture was stirred overnight
  5. concentrationThe product was concentrated
  6. custompurified by preparative HPLC

Sources & evidence

ORD record
ord-767e7a3271304c979a0bc387c7578355
Source dataset
uspto-grants-2011_08
DOI
10.6084/m9.figshare.5104873.v1
Patent number
US07994209B2

Reaction notes

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On this pageParticipantsConditionsProcedureWorkupSources & evidenceReaction notes