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Cyclohexane → (2,2-Difluoro-1,3-dioxaindan-4-yl)boronic acid

HRID 527654
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HRID 527654 반응식
[F:1][C:2]1([F:11])[O:6][C:5]2[CH:7]=[CH:8][CH:9]=[CH:10][C:4]=2[O:3]1.C1CCCCC1.[Li]C(CC)C.C[O:24][B:25](OC)[O:26]C>C1COCC1>[F:11][C:2]1([F:1])[O:3][C:4]2[CH:10]=[CH:9][CH:8]=[C:7]([B:25]([OH:26])[OH:24])[C:5]=2[O:6]1
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참가 물질

6

반응물 4

HCID 8078Cyclohexane2회HCID 8470Trimethyl borateHCID 741032,2-Difluoro-1,3-benzodioxoleHCID 178418400CID 53628100

생성물 1

HCID 16427145(2,2-Difluoro-1,3-dioxaindan-4-yl)boronic acid

시약·촉매·용매 1

HCID 8028Tetrahydrofuran용매

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온도
-78 °C

실험 절차

2,2-Difluoro-1,3-benzodioxole (960 mg, 6.1 mmol) was dissolved in THF (8 mL) and cyclohexane (4 mL) and the resulting solution cooled to −78° C. sec-BuLi 1.4M solution in cyclohexane (4.3 mL, 6.1 mmol) was added dropwise and the reaction mixture stirred for 1.5 hours at −78° C. Trimethylborate (694 mg, 6.75 mmol) was added and the mixture was allowed to warm slowly to −30° C. The reaction mixture was quenched with a 2N solution of HCl and diluted with ethyl acetate. Two phases were separated and the organic layer was washed twice with brine, dried over Na2SO4 and evaporated to dryness affording the title compound as yellow oil which was used in the next step without further purification.

후처리

  1. additionwas added dropwise
  2. temperatureto warm slowly to −30° C
  3. customThe reaction mixture was quenched with a 2N solution of HCl
  4. additiondiluted with ethyl acetate
  5. customTwo phases were separated
  6. washthe organic layer was washed twice with brine
  7. dry with materialdried over Na2SO4
  8. customevaporated to dryness

출처 및 근거

ORD 기록
ord-b907f949b4e64d55a871ba2d671a0e6b
출처 데이터셋
uspto-grants-2016_05
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US09346790B2

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