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Aniline → (R)-methyl 2-phenyl-2-(phenylamino)acetate

HRID 76965
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인쇄 미리보기

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HRID 76965 반응식
[NH2:1][C:2]1[CH:7]=[CH:6][CH:5]=[CH:4][CH:3]=1.CS(O[C@@H:13]([C:18]1[CH:23]=[CH:22][CH:21]=[CH:20][CH:19]=1)[C:14]([O:16][CH3:17])=[O:15])(=O)=O>CC#N>[C:18]1([C@@H:13]([NH:1][C:2]2[CH:7]=[CH:6][CH:5]=[CH:4][CH:3]=2)[C:14]([O:16][CH3:17])=[O:15])[CH:23]=[CH:22][CH:21]=[CH:20][CH:19]=1
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참가 물질

4

반응물 2

HCID 6115AnilineHCID 10999262(S)-methyl 2-(methylsulfonyloxy)-2-phenylacetate

생성물 1

HCID 11514250(R)-methyl 2-phenyl-2-(phenylamino)acetate수율 92%

시약·촉매·용매 1

HCID 6342Acetonitrile용매

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온도
120 °C

실험 절차

Aniline (16.8 mL, 184 mmol) is added to a solution of (S)-methyl 2-(methylsulfonyloxy)-2-phenylacetate (I5) (22.4 g, 92.0 mmol) in CH3CN (50 mL). The mixture is heated under MW irradiation at 120° C. for 5 minutes (UPLC-MS monitoring: complete conversion). The resulting crude is partitioned between EtOAc (200 mL) and 1N HCl (200 mL) and the aqueous phase is extracted with EtOAc (3×200 mL). The combined organic layers are dried over Na2SO4, filtered and evaporated under vacuum to obtain 20.3 g of a pale yellow solid (92% yield), which is used in the next step without any additional purification.

후처리

  1. customThe resulting crude is partitioned between EtOAc (200 mL) and 1N HCl (200 mL)
  2. extractionthe aqueous phase is extracted with EtOAc (3×200 mL)
  3. dry with materialThe combined organic layers are dried over Na2SO4
  4. filtrationfiltered
  5. customevaporated under vacuum

출처 및 근거

ORD 기록
ord-0ad078fcfe7a4e599117c5c8a2647570
출처 데이터셋
uspto-grants-2014_09
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US08835682B2

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