반응 #53821

ord-8862db1a54a94de0908797be4694ab12

반응 방정식

CN(C(=O)Oc1ccc(F)c(F)c1)[C@H]1CC[C@H](O)CC1
trans-(4-Hydroxy-cyclohexyl)-methyl-carbamic acid 3,4-difluoro-phenyl ester
[Na+].[OH-]
NaOH
BrCCCCBr
1,4-dibromobutane
CN(C(=O)Oc1ccc(F)c(F)c1)[C@H]1CC[C@H](OCCCCBr)CC1
trans-[4-(4-bromo-butoxy)-cyclohexyl]-methyl-carbamic acid 3,4-difluoro-phenyl ester
수율 31.0%

반응 조건

상세 조건
See reaction.notes.procedure_details.

후처리

  1. 1
    추출The reaction was extracted (CH2Cl2 2×)
  2. 2
    건조The organic phase was dried over Na2SO4
  3. 3
    기타evaporated
  4. 4
    기타purified by flash silica gel column (first with hexane
  5. 5
    기타to remove the dibromobutane

실험 절차

A solution of 11.6 g (containing 31 mmol) of crude trans-(4-Hydroxy-cyclohexyl)-methyl-carbamic acid 3,4-difluoro-phenyl ester in 110 ml of 1,4-dibromobutane was treated with 3.16 g (9.3 mmol) tetrabutylammonium hydrogen sulfate and 200 ml of aqueous 50% NaOH and stirred for 2.5 days at RT. The reaction was extracted (CH2Cl2 2×). The organic phase was dried over Na2SO4, evaporated and purified by flash silica gel column (first with hexane to remove the dibromobutane and then hexane/EtOAc 1:1) to yield 4.06 g (31%) of trans-[4-(4-bromo-butoxy)-cyclohexyl]-methyl-carbamic acid 3,4-difluoro-phenyl ester, MS: 420 (M, 1Br).

출처

DOI: 10.6084/m9.figshare.5104873.v1특허: US06858651B2uspto-grants-2005_02