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Triethyl borate → B-2,1,3-Benzoxadiazol-4-ylboronic acid

HRID 369037
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HRID 369037 반응식
[N:1]1[O:2][N:3]=[C:4]2[C:9](Br)=[CH:8][CH:7]=[CH:6][C:5]=12.C([O:13][B:14](OCC)[O:15]CC)C.[Li]CCCC.[Cl-].[NH4+]>O1CCCC1.CCCCC>[N:1]1[O:2][N:3]=[C:4]2[C:9]([B:14]([OH:15])[OH:13])=[CH:8][CH:7]=[CH:6][C:5]=12
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참가 물질

7

반응물 4

HCID 9009Triethyl borateHCID 25517Ammonium ChlorideHCID 6078234-Bromo-2,1,3-benzoxadiazoleHCID 178418339Butyllithium

생성물 1

HCID 21186805B-2,1,3-Benzoxadiazol-4-ylboronic acid수율 32%

시약·촉매·용매 2

HCID 8003Pentane용매
HCID 8028
Tetrahydrofuran
용매

실험 절차

To a solution of 4-benzo[c]furazanyl bromide (4 g, 0.020 mol) in tetrahydrofurane (80 ml) and n-pentane (20 ml) is added triethylborate (3.8 ml, 0.022 mol) and N,N,N,N-tetraethylendiamine (3 ml, 0.02 mol). Then, n-BuLi (8.8 ml, 2.5N in hexane, 0.022 mol) is added dropwise at -100° C. and the solution is stirred for 5 minutes more. The reaction mixture is poured into an aqueous solution of saturated ammonium chloride and the water phase is extracted with ethyl acetate. The organic solvent is removed and the crude product is taken up in dichloromethan/n-hexane (5:6). The suspension is filtered to yield the title compound (1.05 g) which is used without further purification.

후처리

  1. extractionthe water phase is extracted with ethyl acetate
  2. customThe organic solvent is removed
  3. filtrationThe suspension is filtered

출처 및 근거

ORD 기록
ord-4ebbced45bb6440c905812d638390ec3
출처 데이터셋
uspto-grants-2000_10
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US06136821

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