Hexane → HCID 58017222, compound

HRID 1895053Notes

Reaction equation

HRID 1895053 reaction equation
[F:1][C:2]1[C:10]2[S:9][CH:8]=[CH:7][C:6]=2[CH:5]=[CH:4][CH:3]=1.[Li]CCCC.CCCCCC.[C:22]([O:26][C:27]([N:29]1[CH2:33][CH2:32][C:31]([CH:41]=[O:42])([CH2:34][CH:35]2[CH2:40][CH2:39][O:38][CH2:37][CH2:36]2)[CH2:30]1)=[O:28])([CH3:25])([CH3:24])[CH3:23]>O1CCCC1>[C:22]([O:26][C:27]([N:29]1[CH2:33][CH2:32][C:31]([CH:41]([C:8]2[S:9][C:10]3[C:2]([F:1])=[CH:3][CH:4]=[CH:5][C:6]=3[CH:7]=2)[OH:42])([CH2:34][CH:35]2[CH2:40][CH2:39][O:38][CH2:37][CH2:36]2)[CH2:30]1)=[O:28])([CH3:24])([CH3:25])[CH3:23]

Participants

6

Reactant 4

HCID 8058HexaneHCID 218660597-Fluoro-1-benzothiopheneHCID 58017286HCID 58017286, compoundHCID 178418339Butyllithium

Product 1

HCID 58017222HCID 58017222, compoundYield 30.4%

Reagents, catalysts & solvents 1

HCID 8028TetrahydrofuranSolvent2×

Conditions

Temperature
-78 °C

Procedure

To a solution of 7-fluoro-benzothiophene (0.22 g, 1.44 mmoles) in anhydrous tetrahydrofuran (10 ml) at −78° C. was added dropwise a solution of n-BuLi in hexane (1.6M, 0.9 ml, 1.44 mmoles). The reaction mixture was stirred at −78° C. for one hour, and then a solution of 3-formyl-3-(tetrahydro-pyran-4-ylmethyl)-pyrrolidine-1-carboxylic acid tert-butyl ester (0.3 g, 1.01 mmoles) in anhydrous tetrahydrofuran (5 ml) was then added. The reaction mixture was stirred at −78° C. for 3 hours, quenched with saturated aqueous ammonium chloride, and partitioned between ethyl acetate and saturated aqueous ammonium chloride solution. The organic phase was washed with brine, dried over anhydrous sodium sulfate, filtered, and concentrated under reduced pressure. The residue was purified by silica gel chromatography (10 to 45% ethyl acetate in hexane) to yield 3-[(7-Fluoro-benzo[b]thiophen-2-yl)-hydroxy-methyl]-3-(tetrahydro-pyran-4-ylmethyl)-pyrrolidine-1-carboxylic acid tert-butyl ester as a colorless semisolid (0.138 g, 30%). MS=450 [M+H]+.

Workup

  1. stirringThe reaction mixture was stirred at −78° C. for 3 hours
  2. customquenched with saturated aqueous ammonium chloride
  3. custompartitioned between ethyl acetate and saturated aqueous ammonium chloride solution
  4. washThe organic phase was washed with brine
  5. dry with materialdried over anhydrous sodium sulfate
  6. filtrationfiltered
  7. concentrationconcentrated under reduced pressure
  8. customThe residue was purified by silica gel chromatography (10 to 45% ethyl acetate in hexane)

Sources & evidence

ORD record
ord-e63599ce075d432092592f7b84b2db76
Source dataset
uspto-grants-2013_08
Patent number
US08513425B2

Reaction notes

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