Ammonium Chloride → HCID 86649678, 화합물

HRID 1911248노트

반응식

HRID 1911248 반응식
[Na].[N:2]([CH2:5][C:6]([O:8][CH2:9][CH3:10])=[O:7])=[N+:3]=[N-:4].[CH3:11][Si:12]([CH3:22])([CH3:21])[C:13]1[CH:14]=[C:15]([CH:18]=[CH:19][CH:20]=1)[CH:16]=O.[NH4+].[Cl-]>CCO>[N:2]([C:5](=[CH:16][C:15]1[CH:18]=[CH:19][CH:20]=[C:13]([Si:12]([CH3:11])([CH3:22])[CH3:21])[CH:14]=1)[C:6]([O:8][CH2:9][CH3:10])=[O:7])=[N+:3]=[N-:4]

참가 물질

6

반응물 4

HCID 25517Ammonium ChlorideHCID 69480Acetic acid, azido-, ethyl esterHCID 5360545SodiumHCID 11823172HCID 11823172, 화합물

생성물 1

HCID 86649678HCID 86649678, 화합물수율 26.9%

시약·촉매·용매 1

HCID 702Ethanol용매2회

반응 조건

온도
-10 °C

실험 절차

To a solution of 2 g (87.5 mmol) of sodium in 30 mL of anhydrous EtOH, maintained under a nitrogen atmosphere and cooled to −10° C., is added, dropwise, a mixture of 31.4 mL (87.5 mmol) of ethyl azidoacetate (at 34% in CH2Cl2) and 3.9 g (21.87 mmol) of 3-trimethylsilylbenzaldehyde prepared according to the procedure described in the preceding step, diluted with 3 mL of EtOH. The reaction mixture is stirred at 0° C. for 4 hours. It is then hydrolysed by adding, with vigorous stirring, 100 mL of aqueous NH4Cl solution (30%). The aqueous phase is extracted with 3×50 mL of EtOAc. The combined organic phases are washed with water, dried over Na2SO4 and concentrated under reduced pressure. The crude reaction product is purified by chromatography on a column of silica gel, eluting with an isocratic mixture of heptane and CH2Cl2 (80/20). 1.7 g of the expected ethyl 2-azido-3-(3-trimethylsilylphenyl)propenoate are thus isolated in the form of a yellow oil.

후처리

  1. additionis added
  2. customprepared
  3. extractionThe aqueous phase is extracted with 3×50 mL of EtOAc
  4. washThe combined organic phases are washed with water
  5. dry with materialdried over Na2SO4
  6. concentrationconcentrated under reduced pressure
  7. customThe crude reaction product
  8. customis purified by chromatography on a column of silica gel
  9. washeluting with an isocratic mixture of heptane and CH2Cl2 (80/20)

출처 및 근거

ORD 기록
ord-9e52278c047a46758aab4e8a6f4a9984
출처 데이터셋
uspto-grants-2013_12
특허 번호
US08604050B2

반응 노트

불러오는 중…