Sodium Bicarbonate → (S)-oxiranylmethyl-carbamic acid benzyl ester

HRID 2228862노트

반응식

HRID 2228862 반응식
[CH2:1]([O:8][C:9](=[O:16])[NH:10][CH2:11][C@H:12]([OH:15])[CH2:13]O)[C:2]1[CH:7]=[CH:6][CH:5]=[CH:4][CH:3]=1.C([O-])(O)=O.[Na+].C[O-].[Na+]>C(Cl)(Cl)Cl>[CH2:1]([O:8][C:9](=[O:16])[NH:10][CH2:11][C@@H:12]1[O:15][CH2:13]1)[C:2]1[CH:7]=[CH:6][CH:5]=[CH:4][CH:3]=1

참가 물질

5

반응물 3

HCID 516892Sodium Bicarbonate2회HCID 10942334Sodium MethoxideHCID 11310670benzyl N-[(2S)-2,3-dihydroxypropyl]carbamate

생성물 1

HCID 10375722(S)-oxiranylmethyl-carbamic acid benzyl ester수율 90%

시약·촉매·용매 1

HCID 6212Chloroform용매

실험 절차

(S)-2,3-Dihydroxy-1-propylcarbamate benzyl ester (2.11 g, 0.01 mol) in 100 ml flask was dissolved in CHCl3 (30 ml). 1-Chlorocarbonyl-1-methylethylacetate (1.8 ml, 0.013 mol) was added and stirred for 3 hours at ambient temperature. Sat. aqueous solution of NaHCO3 (20 ml) was added and extracted three times with ethyl acetate (50 ml). The organic layer was evaporated and dissolved in THF (50 ml). Sodium methoxide (0.53 g, 0.01 mol) was added and stirred for 6 hours. Sat. aqueous solution of NaHCO3 (50 ml) was added and extracted with ethyl acetate (50 ml). The organic layer was dried over anhydrous MgSO4 and evaporated to dryness. The crude product was purified by column chromatography on silica gel to give (S)-2,3-epoxy-1-propylcarbamate benzyl ester (90%, optical purity>99%ee).

후처리

  1. extractionextracted three times with ethyl acetate (50 ml)
  2. customThe organic layer was evaporated
  3. dissolutiondissolved in THF (50 ml)
  4. stirringstirred for 6 hours
  5. extractionextracted with ethyl acetate (50 ml)
  6. dry with materialThe organic layer was dried over anhydrous MgSO4
  7. customevaporated to dryness
  8. customThe crude product was purified by column chromatography on silica gel

출처 및 근거

ORD 기록
ord-7fce327d3be8414bab7091212ab0b61d
출처 데이터셋
uspto-grants-2002_07
특허 번호
US06417403B1

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