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Hydrochloric Acid → (5-Methylthiophen-2-yl)boronic acid

HRID 497166
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HRID 497166 반응식
Br[C:2]1[S:3][C:4]([CH3:7])=[CH:5][CH:6]=1.[Li]CCCC.C[O:14][B:15](OC)[O:16]C.Cl>C1COCC1>[CH3:7][C:4]1[S:3][C:2]([B:15]([OH:16])[OH:14])=[CH:6][CH:5]=1
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

6

반응물 4

HCID 313Hydrochloric AcidHCID 8470Trimethyl borateHCID 698312-Bromo-5-methylthiopheneHCID 178418339Butyllithium

생성물 1

HCID 2734374(5-Methylthiophen-2-yl)boronic acid수율 67.9%

시약·촉매·용매 1

HCID 8028Tetrahydrofuran용매

실험 절차

To a stirred solution of 2-bromo-5-methylthiophene (2.5 g, 14.1 mmol) in THF (30 mL) was added n-BuLi (1.55 M solution in hexane, 10.0 mL, 15.5 mmol) at −78° C. under nitrogen, and the mixture was stirred for 1 hour. Trimethylborate (1.83 g, 17.6 mmol) was added to the mixture, and residue was allowed to warm up to room temperature overnight. The reaction mixture was cooled at 0° c and 2N HCl (10 mL) was added, and the mixture was stirred for 1 hour. The organic layer was separated and the aqueous layer was extracted with diethylether. The combined organic layer was washed with brine, dried over MgSO4, and concentrated in vacuo, to give the title compound (1.36 g).

후처리

  1. additionwas added
  2. stirringthe mixture was stirred for 1 hour
  3. customThe organic layer was separated
  4. extractionthe aqueous layer was extracted with diethylether
  5. washThe combined organic layer was washed with brine
  6. dry with materialdried over MgSO4
  7. concentrationconcentrated in vacuo

출처 및 근거

ORD 기록
ord-0cb2544ca0b44929ac5ba89ca80db0a8
출처 데이터셋
uspto-grants-2005_09
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US06949536B2

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