Formaldehyde → (R)-5-Biphenyl-4-ylmethyl-3-methylene-2-oxo-pyrrolidine-1-carboxylic acid tert-butylester

HRID 2179522Notes

Reaction equation

HRID 2179522 reaction equation
[C:1]([C@@H:9]1[CH2:13][CH:12]([CH2:14][C:15]2[CH:20]=[CH:19][C:18]([C:21]3[CH:26]=[CH:25][CH:24]=[CH:23][CH:22]=3)=[CH:17][CH:16]=2)[N:11](/C=C/C2C=CC=CC=2)[C:10]1=[O:35])(=O)C1C=CC=CC=1.[CH2:36]=O.[OH-].C([N+](C[CH2:53][CH2:54][CH3:55])(CCCC)CCCC)CCC.[C:56]([O-:59])([O-])=[O:57].[K+].[K+]>O1CCCC1.[Cl-].[Na+].O>[C:54]([O:59][C:56]([N:11]1[C@H:12]([CH2:14][C:15]2[CH:16]=[CH:17][C:18]([C:21]3[CH:22]=[CH:23][CH:24]=[CH:25][CH:26]=3)=[CH:19][CH:20]=2)[CH2:13][C:9](=[CH2:1])[C:10]1=[O:35])=[O:57])([CH3:53])([CH3:55])[CH3:36]

Participants

7

Reactant 4

HCID 712FormaldehydeHCID 11430Potassium CarbonateHCID 2723671Tetrabutylammonium HydroxideHCID 86673650HCID 86673650, compound

Product 1

HCID 46193438(R)-5-Biphenyl-4-ylmethyl-3-methylene-2-oxo-pyrrolidine-1-carboxylic acid tert-butylester

Reagents, catalysts & solvents 2

HCID 8028TetrahydrofuranSolventHCID 57417360Sodium chloride; waterSolvent

Conditions

Temperature
50 °C

Procedure

The mixture of (R/S)-3-(2,2-dimethyl-propionyl)-(S)-5-biphenyl-4-ylmethyl-2-oxo-pyrrolidine-1-carboxylic acid tert-butyl ester 4a, R1=t-butoxycarbonyl, R4=t-butyl) (0.87 g, 2 mmol), formaldehyde (37% in water, 0.49 g, 6 mmol), tetrabutyl ammonium hydroxide (26 mg, 0.1 mmol) and K2CO3 (0.55 g, 1.3 mmol, dissolved in 2 mL water) in 10 mL dry tetrahydrofuran was heated to 50° C. and stirred for 2 hours. Then the reaction mixture is diluted with 10 mL brine and stirred for 15 min, stop stirring, and remove the lower aqueous layer. the organic phase is then concentrated in vacuo. ethyl acetate 20 mL is added, filtered and the filtrate concentrated and purified by column chromatography eluting with 5:1 heptane/ethyl acetate to afford (R)-5-Biphenyl-4-ylmethyl-3-methylene-2-oxo-pyrrolidine-1-carboxylic acid tert-butylester (1a, R1=t-butoxycarbonyl). Spectroscopic data as reported in WO2009/090251 (Example 23, Method 1).

Workup

  1. stirringstirred for 15 min
  2. stirringstop stirring
  3. customremove the lower aqueous layer
  4. concentrationthe organic phase is then concentrated in vacuo
  5. additionethyl acetate 20 mL is added
  6. filtrationfiltered
  7. concentrationthe filtrate concentrated
  8. custompurified by column chromatography
  9. washeluting with 5:1 heptane/ethyl acetate

Sources & evidence

ORD record
ord-de2c3a00e8bd4f0dad6cde2a1931b4e1
Source dataset
uspto-grants-2015_06
Patent number
US09067883B2

Reaction notes

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