Benzyl Bromide → Boc-Ser-OBzl

HRID 2217143

반응식

HRID 2217143 반응식
[C:1]([NH:8][C@H:9]([C:12]([OH:14])=[O:13])[CH2:10][OH:11])([O:3][C:4]([CH3:7])([CH3:6])[CH3:5])=[O:2].[CH2:15](Br)[C:16]1[CH:21]=[CH:20][CH:19]=[CH:18][CH:17]=1.C(=O)([O-])[O-].[Cs+].[Cs+]>CN(C=O)C>[CH2:15]([O:13][C:12](=[O:14])[C@H:9]([CH2:10][OH:11])[NH:8][C:1]([O:3][C:4]([CH3:7])([CH3:6])[CH3:5])=[O:2])[C:16]1[CH:21]=[CH:20][CH:19]=[CH:18][CH:17]=1

참가 물질

5

반응물 3

HCID 7498Benzyl BromideHCID 10796Cesium carbonateHCID 98766N-[tert-butoxycarbonyl]-L-serine

생성물 1

HCID 7018792Boc-Ser-OBzl

시약·촉매·용매 1

HCID 6228Dimethylformamide용매

실험 절차

In a round-bottomed flask were placed N-BocSerine (20.0 g, 89.605 mmol, 1 eq.), benzyl bromide (10.76 ml, 90.50 mmol, 1.01 eq.) and cesium carbonate (56.64 g, 173.84 mmol, 1.94 eq.) in DMF (180 mL). The suspension was stirred under nitrogen at room temperature for 2 hrs to overnight. The mixture was partitioned between water and ethyl acetate (1:1, 1000 ml) and aqueous layer was re-extracted with ethyl acetate (2×200 mL). The combined organic layers were washed with water (2×500 mL), saturated sodium chloride, and dried over sodium sulfate. The solvents were removed in vacuo and the crude material purified on silica gel to get N-Boc-serine benzyl ester.

후처리

  1. customIn a round-bottomed flask were placed
  2. customThe mixture was partitioned between water and ethyl acetate (1:1, 1000 ml) and aqueous layer
  3. extractionwas re-extracted with ethyl acetate (2×200 mL)
  4. washThe combined organic layers were washed with water (2×500 mL), saturated sodium chloride
  5. dry with materialdried over sodium sulfate
  6. customThe solvents were removed in vacuo
  7. customthe crude material purified on silica gel

출처 및 근거

ORD 기록
ord-257c1248422141ba8cd742f14136ac78
출처 데이터셋
uspto-grants-2008_08
특허 번호
US07407952B2

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