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Sodium Hydroxide → 1-[(2-Bromophenyl)sulfanyl]cyclohexanecarboxylic acid

HRID 1744083
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반응식

HRID 1744083 반응식
[Br:1][C:2]1[CH:7]=[CH:6][CH:5]=[CH:4][C:3]=1[S:8][C:9]1([C:15]([O:17]C)=[O:16])[CH2:14][CH2:13][CH2:12][CH2:11][CH2:10]1.[OH-].[Na+]>CO>[Br:1][C:2]1[CH:7]=[CH:6][CH:5]=[CH:4][C:3]=1[S:8][C:9]1([C:15]([OH:17])=[O:16])[CH2:14][CH2:13][CH2:12][CH2:11][CH2:10]1
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

4

반응물 2

HCID 14798Sodium HydroxideHCID 22235978Methyl 1-[(2-bromophenyl)sulfanyl]cyclohexanecarboxylate

생성물 1

HCID 222359741-[(2-Bromophenyl)sulfanyl]cyclohexanecarboxylic acid

시약·촉매·용매 1

HCID 887Methanol용매

실험 절차

To a solution of methyl 1-[(2-bromophenyl)sulfanyl]cyclohexanecarboxylate (89 mg, in MeOH (3 mL) was added 1 M NaOH (1 mL). The mixture was stirred at room temperature for 2 days, then at 65° C. for 6 h. The mixture was then concentrated and the residue was partitioned between ethyl acetate and 1 M HCl. The organic phase was washed with brine, dried over MgSO4 and concentrated to give 1-[(2-bromophenyl)sulfanyl]cyclohexanecarboxylic acid.

후처리

  1. waitat 65° C. for 6 h
  2. concentrationThe mixture was then concentrated
  3. customthe residue was partitioned between ethyl acetate and 1 M HCl
  4. washThe organic phase was washed with brine
  5. dry with materialdried over MgSO4
  6. concentrationconcentrated

출처 및 근거

ORD 기록
ord-e8eae0de17334900a2de9109a72d20fd
출처 데이터셋
uspto-grants-2006_03
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US07012075B2

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