تفاعل #674293

ord-f4d7eef048244bc79c788878e5fb1d8b

معادلة التفاعل

[Cl-].[NH4+]
NH4Cl
CC(C)(C)OC(=O)N1CC2(CC(O)C2)C1
tert-Butyl 6-hydroxy-2-azaspiro[3.3]heptane-2-carboxylate
CCN(CC)CC
Et3N
CS(=O)(=O)Cl
Methanesulfonyl chloride
CC(C)(C)OC(=O)N1CC2(CC(OS(C)(=O)=O)C2)C1
tert-butyl 6-((methylsulfonyl)oxy)-2-azaspiro[3.3]heptane-2-carboxylate
المردود 99.1%

المذيبات

ظروف التفاعل

درجة الحرارة
0°CELSIUS
الظروف التفصيلية
See reaction.notes.procedure_details.

المعالجة

  1. 1
    درجة الحرارةto warm to room temperature
  2. 2
    workup.STIRRINGstirred at room temperature for 18 hrs
  3. 3
    workup.STIRRINGstirred at room temperature for 10 min
  4. 4
    أخرىThe layers were separated
  5. 5
    استخلاصThe aqueous phase was extracted with DCM (3×30 mL)
  6. 6
    تجفيفThe combined organic phase was dried over anhydrous Na2SO4
  7. 7
    تركيزconcentrated by evaporation in vacuo

الإجراء التجريبي

tert-Butyl 6-hydroxy-2-azaspiro[3.3]heptane-2-carboxylate (505 mg, 2.37 mmol) was dissolved in DCM (6.0 mL). The solution was cooled to 0° C. with an external ice-bath. Et3N (330 μL, 2.37 mmol) and DMAP (3.0 mg, 0.0237 mmol) were added. Methanesulfonyl chloride (184 μL, 2.37 mmol) was then added dropwise by syringe. The solution was stirred at 0° C. for 2.0 hrs, was then allowed to warm to room temperature and stirred at room temperature for 18 hrs. A saturated solution of NH4Cl (20 mL) was added and stirred at room temperature for 10 min. The layers were separated. The aqueous phase was extracted with DCM (3×30 mL). The combined organic phase was dried over anhydrous Na2SO4, concentrated by evaporation in vacuo to afford tert-butyl 6-((methylsulfonyl)oxy)-2-azaspiro[3.3]heptane-2-carboxylate (684 mg, 99%) as a white solid.

المصدر

DOI: 10.6084/m9.figshare.5104873.v1براءة الاختراع: US09226923B2uspto-grants-2016_01