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Hydrochloric Acid → HCID 86727239, 화합물

HRID 2173027
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HRID 2173027 반응식
[F:1][C:2]1[C:10]2[CH:9]=[CH:8][S:7][C:6]=2[CH:5]=[CH:4][CH:3]=1.C([Li])CCC.[B:16](OC(C)C)([O:21]C(C)C)[O:17]C(C)C.Cl>C1COCC1.C(Cl)Cl>[F:1][C:2]1[C:10]2[CH:9]=[C:8]([B:16]([OH:21])[OH:17])[S:7][C:6]=2[CH:5]=[CH:4][CH:3]=1
참가 물질반응 조건실험 절차후처리출처 및 근거반응 노트

참가 물질

7

반응물 4

HCID 313Hydrochloric AcidHCID 21531Triisopropyl borateHCID 190880174-Fluorobenzo[b]thiopheneHCID 178418339Butyllithium

생성물 1

HCID 86727239HCID 86727239, 화합물

시약·촉매·용매 2

HCID 6344Dichloromethane용매
HCID 8028
Tetrahydrofuran
용매

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온도
-78 °C

실험 절차

To a cold (−78° C.) solution of 4-fluorobenzo[b]thiophene (80.4 mg, 0.528 mmol) in anhydrous THF (1 mL) was added n-butyllithium (0.363 mL, 0.581 mmol) dropwise. The reaction mixture was stirred at −78° C. for 60 minutes. A solution of triisopropyl borate (0.146 mL, 0.634 mmol) was added. The reaction mixture was stirred at −78° C. for 30 minutes and was then allowed to warm to room temperature over a 2 hour period. TLC showed completion of reaction. 1N HCl (100 mL) and DCM (50 mL) were added to the reaction mixture. The aqueous and organic layers were separated. The aqueous layer was concentrated to 50 mL, yielding a solid precipitate that was filtered and dried to give the title compound as off-white, needle-shaped crystals. The product was used without further purification.

후처리

  1. stirringThe reaction mixture was stirred at −78° C. for 30 minutes
  2. temperatureto warm to room temperature over a 2 hour period
  3. customcompletion of reaction
  4. customThe aqueous and organic layers were separated
  5. concentrationThe aqueous layer was concentrated to 50 mL
  6. customyielding a solid precipitate that
  7. filtrationwas filtered
  8. customdried

출처 및 근거

ORD 기록
ord-164e0292e44948e3be73df1b8946ecb2
출처 데이터셋
uspto-grants-2015_06
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US09056873B2

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