تفاعل #987

ord-991308a13d764cc0817ac696051b408e

معادلة التفاعل

Cl
HCl
CC(C)(C)[Si](OCc1ccc(CCCC2OCCO2)cc1)(c1ccccc1)c1ccccc1
dioxolane
CC(C)(C)[Si](OCc1ccc(CCCC2OCCO2)cc1)(c1ccccc1)c1ccccc1
2-[3-(4-tert-Butyldiphenylsilyloxymethylphenyl)propyl]-[1,3]-dioxolane
Cl
HCl
c1c[nH]cn1
imidazole
CC(C)(C)[Si](Cl)(c1ccccc1)c1ccccc1
tert-butylchlorodiphenyl silane
O=C([O-])[O-].[K+].[K+]
K2CO3
CC(C)(C)[Si](OCc1ccc(CCCC=O)cc1)(c1ccccc1)c1ccccc1
aldehyde
المردود 42.8%
CC(C)(C)[Si](OCc1ccc(CCCC=O)cc1)(c1ccccc1)c1ccccc1
4-(4-tert-Butyldiphenylsilyloxymethyl-phenyl)butyraldehyde
المردود 42.8%

المذيبات

ظروف التفاعل

الظروف التفصيلية
See reaction.notes.procedure_details.

المعالجة

  1. 1
    استخلاصextracted with ethyl acetate
  2. 2
    تركيزconcentrated
  3. 3
    workup.DISSOLUTIONThe crude mixture was dissolved into 25 mL of CH2Cl2 to which
  4. 4
    workup.STIRRINGto stir overnight at room temperature
  5. 5
    استخلاصextracted with ethyl acetate
  6. 6
    تجفيفThe organics were dried over MgSO4
  7. 7
    ترشيحfiltered
  8. 8
    تركيزconcentrated
  9. 9
    غسيلFlash chromatography (elution with 8% ethyl acetate in hexane)

الإجراء التجريبي

To a solution of 5.5 g (11.9 mmol) of the dioxolane 171 in 40 mL of THF at room temperature was added 40 mL of 4.0N HCl and the resulting solution was allowed to stir for 1 h. The mixture was neutralized with solid K2CO3, extracted with ethyl acetate and concentrated. The crude mixture was dissolved into 25 mL of CH2Cl2 to which was added 600 mg (8.8 mmol) of imidazole and 1.9 mL (7.3 mmol) of tert-butylchlorodiphenyl silane. The resulting mixture was allowed to stir overnight at room temperature and was then poured into 0.5N HCl and extracted with ethyl acetate. The organics were dried over MgSO4, filtered and concentrated. Flash chromatography (elution with 8% ethyl acetate in hexane) gave 2.12 g of the aldehyde 172 as an oil. 1H NMR consistent with the product.

المصدر

DOI: 10.6084/m9.figshare.5104873.v1براءة الاختراع: US05723459uspto-grants-1998_03