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Hydrochloric Acid → HCID 86727239、化合物

HRID 2173027
ノート
印刷プレビュー

反応式

HRID 2173027 の反応式
[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
参加物反応条件実験手順後処理出典と根拠反応ノート

参加物

7

反応物 4

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

生成物 1

HCID 86727239HCID 86727239、化合物

試薬・触媒・溶媒 2

HCID 6344Dichloromethane溶媒
HCID 8028
Tetrahydrofuran
溶媒

反応条件

温度
-78 °C

実験手順

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.

後処理

  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

出典と根拠

ORDレコード
ord-164e0292e44948e3be73df1b8946ecb2
出典データセット
uspto-grants-2015_06
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US09056873B2

反応ノート

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