تفاعل #1885043

ord-0defb71c850444a991af8b145cdd8207

معادلة التفاعل

O=C(O)C(O)C(O)C(=O)O.[K].[Na]
sodium potassium tartaric acid
CC(C)(C)[Si](O[C@@H]1CCOC1=O)(c1ccccc1)c1ccccc1
(R)-3-(tert-butyldiphenylsilyloxy)-dihydrofuran-2(3H)-one
Nc1ccccc1
aniline
[CH3][Al]([CH3])[CH3]
trimethylaluminum
CC(C)(C)[Si](O[C@H](CCO)C(=O)Nc1ccccc1)(c1ccccc1)c1ccccc1
(R)-2-(tert-butyldiphenylsilyloxy)-4-hydroxy-N-phenylbutanamide
المردود 78.4%

المذيبات

ظروف التفاعل

الظروف التفصيلية
See reaction.notes.procedure_details.

المعالجة

  1. 1
    workup.STIRRINGthe reaction mixture was stirred at RT for 16 hours
  2. 2
    workup.STIRRINGstirred for 15 min
  3. 3
    أخرىThe layers were separated
  4. 4
    غسيلthe aqueous layer was washed with DCM (4×)
  5. 5
    غسيلThe combined organics were washed with 0.1M HCl (2×), brine
  6. 6
    تجفيفdried over Na2SO4
  7. 7
    أخرىevaporated to dryness
  8. 8
    أخرىPurification by silica gel chromatography (10-30% EtOAc in hexane)

الإجراء التجريبي

To a solution of aniline (356 mg, 348 μL, 3.82 mmol) in DCM (17 mL) was added trimethylaluminum (2.0M, 2.1 mL, 4.2 mmol) dropwise and the reaction mixture was stirred at RT for 40 min. A solution of (R)-3-(tert-butyldiphenylsilyloxy)-dihydrofuran-2(3H)-one (1.00 g, 2.94 mmol) in DCM (12 mL) was added dropwise and the reaction mixture was stirred at RT for 16 hours. The reaction mixture was poured into a saturated solution of sodium potassium tartaric acid and stirred for 15 min. The layers were separated, and the aqueous layer was washed with DCM (4×). The combined organics were washed with 0.1M HCl (2×), brine, dried over Na2SO4 and evaporated to dryness. Purification by silica gel chromatography (10-30% EtOAc in hexane) afforded the (R)-2-(tert-butyldiphenylsilyloxy)-4-hydroxy-N-phenylbutanamide (1.00 g, 78%). LC/MS (10%-99% CH3CN (0.035% TFA)/H2O (0.05% TFA)), m/z: M+1 obs=434.7; tR=2.16 min.

المصدر

DOI: 10.6084/m9.figshare.5104873.v1براءة الاختراع: US08343763B2uspto-grants-2013_01