تفاعل #324439

ord-9837502c913340699380870af8ddc24d

معادلة التفاعل

CC(C)(C)OC(=O)N1CCC(Oc2ccc(Cl)cc2C=O)C1
title compound
CC(C)(C)OC(=O)N1CCC(Oc2ccc(Cl)cc2C=O)C1
3-(4-chloro-2-formyl-phenoxy)-pyrrolidine-1-carboxylic acid tert-butyl ester
O=C(OO)c1cccc(Cl)c1
m-CPBA
CC(C)(C)OC(=O)N1CCC(Oc2ccc(Cl)cc2O)C1
title compound
CC(C)(C)OC(=O)N1CCC(Oc2ccc(Cl)cc2O)C1
3-(4-chloro-2-hydroxy-phenoxy)-pyrrolidine-1-carboxylic acid tert-butyl ester

المذيبات

ظروف التفاعل

الظروف التفصيلية
See reaction.notes.procedure_details.

المعالجة

  1. 1
    غسيلthe reaction washed with saturated NaHCO3 (aq.) and 10% Na2S2O5 until KI paper negative
  2. 2
    أخرىThe combined organic layers were dried
  3. 3
    workup.ADDITIONthen treated with MeOH (25 mL) and 1N NaOH (25 mL)
  4. 4
    workup.WAITAfter 15 h
  5. 5
    استخلاصthen extracted with EtOAc (2×)
  6. 6
    غسيلThe combined organic layers were washed with brine
  7. 7
    أخرىdried

الإجراء التجريبي

To a CH2Cl2 (25 mL) solution of the title compound of Step A (1.4 g, 4.3 mmol) was added 77% m-CPBA (1.4 g, 6.2 mmol). After 18 h, additional CH2Cl2 was added and the reaction washed with saturated NaHCO3 (aq.) and 10% Na2S2O5 until KI paper negative. The combined organic layers were dried then treated with MeOH (25 mL) and 1N NaOH (25 mL). After 15 h, the reaction was acidified with 1M KHSO4 then extracted with EtOAc (2×). The combined organic layers were washed with brine and dried to give the title compound as a white solid. 1H NMR (CDCl3): 6.96 (s, 1H), 6.82-6.80 (m, 1H), 6.73 (d, J=8.6 Hz, 1H), 5.62 (s, 1H), 4.91 (s, 1H), 3.66-3.46 (m, 4H), 2.20-2.11 (m, 2H), 1.47 (s, 9H).

المصدر

DOI: 10.6084/m9.figshare.5104873.v1براءة الاختراع: US08642583B2uspto-grants-2014_02