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Ethyl 3-bromobenzoate → Ethyl 3-(2-(benzyloxymethyl)-2H-tetrazol-5-yl)benzoate

HRID 1016181
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HRID 1016181 반응식
[CH2:1]([O:3][C:4](=[O:12])[C:5]1[CH:10]=[CH:9][CH:8]=[C:7](Br)[CH:6]=1)[CH3:2].[CH2:13]([O:20][CH2:21][N:22]1[N:26]=[N:25][C:24]([Sn](CCCC)(CCCC)CCCC)=[N:23]1)[C:14]1[CH:19]=[CH:18][CH:17]=[CH:16][CH:15]=1>C1(C)C=CC=CC=1.[Cu]I.C1C=CC([P]([Pd]([P](C2C=CC=CC=2)(C2C=CC=CC=2)C2C=CC=CC=2)([P](C2C=CC=CC=2)(C2C=CC=CC=2)C2C=CC=CC=2)[P](C2C=CC=CC=2)(C2C=CC=CC=2)C2C=CC=CC=2)(C2C=CC=CC=2)C2C=CC=CC=2)=CC=1>[CH2:13]([O:20][CH2:21][N:22]1[N:26]=[N:25][C:24]([C:7]2[CH:6]=[C:5]([CH:10]=[CH:9][CH:8]=2)[C:4]([O:3][CH2:1][CH3:2])=[O:12])=[N:23]1)[C:14]1[CH:15]=[CH:16][CH:17]=[CH:18][CH:19]=1
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

6

반응물 2

HCID 90488Ethyl 3-bromobenzoateHCID 113405612-((Phenylmethoxy)methyl)-5-(tributylstannyl)-2H-tetrazole

생성물 1

HCID 57888757Ethyl 3-(2-(benzyloxymethyl)-2H-tetrazol-5-yl)benzoate

시약·촉매·용매 3

HCID 24350Copper(1+) iodide; Copper(I) iodide; Cuprous iodide; Cuprous iodide (CuI)촉매HCID 178418397
HCID 178418397, 화합물
촉매
HCID 1140Toluene용매

실험 절차

A solution of ethyl-3-bromobenzoate (0.47 g, 2.05 mmol) and 2-(benzyloxymethyl)-5-(tributylstannyl)-2H-tetrazole in toluene (20 mL) was degassed under vacuum and argon. To this solution was added copper (I) iodide (20 mg, 0.20 mmol) and tetrakis(triphenylphosphine)palladium(0) (115 mg, 0.10 mmol), and the mixture was again degassed under vacuum and argon. The flask and condenser were covered in foil to exclude light, and the reaction was heated at reflux temperature for 3 hours. After cooling to room temperature, the mixture was filtered and the filtrate was concentrated in-vacuo. The residue was purified over a 3.5×12 cm silica gel column, eluting with 5% then 10% then 15% ethyl acetate/hexanes to yield the title compound as a colorless oil which contained 5% of a tributyltin impurity. MS (ESI+)=339.22, (M+H)+. The oil was used as-is in the next step.

후처리

  1. customthe mixture was again degassed under vacuum and argon
  2. temperaturethe reaction was heated
  3. temperatureat reflux temperature for 3 hours
  4. filtrationthe mixture was filtered
  5. concentrationthe filtrate was concentrated in-vacuo
  6. customThe residue was purified over a 3.5×12 cm silica gel column
  7. washeluting with 5%

출처 및 근거

ORD 기록
ord-84757f6997a64689b082e50bd6480972
출처 데이터셋
uspto-grants-2011_07
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US07985861B2

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