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2-[(4-Nitrophenyl)methanesulfonyl]ethan-1-ol → HCID 15346011, 화합물

HRID 1864074
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HRID 1864074 반응식
[N+:1]([C:4]1[CH:9]=[CH:8][C:7]([CH2:10][S:11]([CH2:14][CH2:15][OH:16])(=[O:13])=[O:12])=[CH:6][CH:5]=1)([O-])=O>CO.[Pd]>[NH2:1][C:4]1[CH:9]=[CH:8][C:7]([CH2:10][S:11]([CH2:14][CH2:15][OH:16])(=[O:13])=[O:12])=[CH:6][CH:5]=1
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

4

반응물 1

HCID 135681992-[(4-Nitrophenyl)methanesulfonyl]ethan-1-ol2회

생성물 1

HCID 15346011HCID 15346011, 화합물수율 37%

시약·촉매·용매 2

HCID 23938Palladium촉매HCID 887Methanol용매

실험 절차

A suspension of 2-{[(4-Nitrophenyl)methyl]sulfonyl}ethanol (Intermediate 148, 7.64 g, 46.3 mmol theoretical) and 10 wt % Pd/C (788 mg) in MeOH was stirred under an atmosphere of H2 at room temperature for 2 h, then filtered through a pad of celite. The filtrate was concentrated in vacuo, and the orange residue was recrystallized from MeOH/Et2O to give the desired product as light yellow crystals (3.65 g, 17.0 mmol, 37% over 3 steps). MS: M(C9H13NO3S)=215.27, (M+H)+=216.0.

후처리

  1. filtrationfiltered through a pad of celite
  2. concentrationThe filtrate was concentrated in vacuo
  3. customthe orange residue was recrystallized from MeOH/Et2O

출처 및 근거

ORD 기록
ord-9394706865dd44449fdebc5520ad54da
출처 데이터셋
uspto-grants-2009_12
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US07625903B2

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