Chlorotrimethylsilane → HCID 86746649, compound

HRID 1614052Notes

Reaction equation

HRID 1614052 reaction equation
FC(F)(F)C(O)=O.C1(C2C3C([N:27]4[CH2:32][CH2:31][CH2:30][C@@H:29]([C:33](=[O:43])[CH2:34][P:35]([O:40]CC)([O:37]CC)=[O:36])[C@@H:28]4[C:44]([O:46][C:47](C)(C)C)=[O:45])=CC=CC=3C3C2=CC=CC=3)C=CC=CC=1.C(=O)([O-])O.[Na+].C[Si](Cl)(C)C>C(#N)C.O.CO.C(O)(C)C>[P:35]([CH2:34][C:33]([C@@H:29]1[CH2:30][CH2:31][CH2:32][NH:27][C@H:28]1[C:44]([O:46][CH3:47])=[O:45])=[O:43])([OH:37])([OH:40])=[O:36]

Participants

9

Procedure

Mix trifluoroacetic acid (30 mL) with acetonitrile (10 mL) and add, by dropwise addition, to an ice-cold solution of N-(9-phenylfluorenyl)-3(R)-[(diethoxyphosphinyl)acetyl]piperidine-2(R)-carboxylic acid, tert-butyl ester (3.5 g, 5.8 mmol) in acetonitrile (40 mL) and water (4 mL). Stir for 15 minutes, warm to room temperature and stir for an additional hour. Pour into saturated aqueous sodium hydrogen carbonate (500 mL) and extract into ethyl acetate (3×200 mL). Evaporate to a residue and take up the residue in acetonitrile (20 mL) and methylene chloride (20 mL). Place under a nitrogen atmosphere and add trimethylsilyl chloride (5 mL, 35 mmol). Stir overnight then add water. Stir for 15 minutes then blow to a residue with a stream of dry nitrogen. Take up the residue in water (100 mL) and wash with toluene (5×100 mL). Freeze dry to give a residue. Take up the residue in methanol (10 mL) and isopropanol (5 mL). Add propylene oxide (5 mL) and filter to give the title compound.

Workup

  1. stirringstir for an additional hour
  2. extractionextract into ethyl acetate (3×200 mL)
  3. customEvaporate to a residue
  4. stirringStir overnight
  5. stirringStir for 15 minutes
  6. washwash with toluene (5×100 mL)
  7. customFreeze dry
  8. customto give a residue
  9. filtrationAdd propylene oxide (5 mL) and filter

Sources & evidence

ORD record
ord-e68f5aebd2db4930bd8015e70df49af6
Source dataset
uspto-grants-1993_03
Patent number
US05194430

Reaction notes

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