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Potassium Acetate → 3-Methyl-3-(4-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)phenyl)thietane 1,1-dioxide

HRID 929261
ノート
印刷プレビュー

反応式

HRID 929261 の反応式
[BH:1]([O:3]BO)[OH:2].O[C:7]([C:10](O)([CH3:12])[CH3:11])([CH3:9])[CH3:8].C([O-])(=O)C.[K+].Br[C:20]1[CH:25]=[CH:24][C:23]([C:26]2([CH3:32])[CH2:29][S:28](=[O:31])(=[O:30])[CH2:27]2)=[CH:22][CH:21]=1>CN(C=O)C.C1C=CC(P(C2C=CC=CC=2)[C-]2C=CC=C2)=CC=1.C1C=CC(P(C2C=CC=CC=2)[C-]2C=CC=C2)=CC=1.Cl[Pd]Cl.[Fe+2].C(Cl)Cl>[CH3:32][C:26]1([C:23]2[CH:24]=[CH:25][C:20]([B:1]3[O:3][C:10]([CH3:12])([CH3:11])[C:7]([CH3:9])([CH3:8])[O:2]3)=[CH:21][CH:22]=2)[CH2:29][S:28](=[O:31])(=[O:30])[CH2:27]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

6

反応物 3

HCID 517044Potassium AcetateHCID 124571823-(4-Bromophenyl)-3-methylthietane 1,1-dioxideHCID 178459140HCID 178459140、化合物

生成物 1

HCID 900421873-Methyl-3-(4-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)phenyl)thietane 1,1-dioxide

試薬・触媒・溶媒 2

HCID 178418807HCID 178418807、化合物触媒
HCID 6228
Dimethylformamide
溶媒

反応条件

温度
90 °C

実験手順

Step D To pinacol diboronate (250 mg, 0.986 mmol), potassium acetate (242 mg, 2.466 mmol) and PdCl2(dppf)-CH2Cl2 adduct (67 mg, 0.082 mmol) in a thick-walled tube was added a solution of 3-(4-bromophenyl)-3-methylthietane 1,1-dioxide (226 mg, from Step C) in DMF (5 ml). The tube was flushed with N2, then capped and heated to 90° C. for 4 hours. Then the reaction was cooled to RT and diluted with EtOAc (30 ml) and water (20 ml). The aqueous layer was separated and extracted with EtOAc (25 ml). The combined organic layers were washed with water (50 ml), dried (Na2SO4), filtered and concentrated. The resulting crude material was purified by Isco™ system, 40 g gold cartridge, 40 ml flow rate, gradient—0/100 (1 min) to 50/50 (19 min) to 50/50 (21 min—total run time) of EtOAc/hexanes. The fractions containing the product were combined and concentrated to provide 3-methyl-3-(4-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)phenyl)thietane 1,1-dioxide as a white solid.

後処理

  1. customThe tube was flushed with N2
  2. customcapped
  3. temperatureThen the reaction was cooled to RT
  4. additiondiluted with EtOAc (30 ml) and water (20 ml)
  5. customThe aqueous layer was separated
  6. extractionextracted with EtOAc (25 ml)
  7. washThe combined organic layers were washed with water (50 ml)
  8. dry with materialdried (Na2SO4)
  9. filtrationfiltered
  10. concentrationconcentrated
  11. customThe resulting crude material was purified by Isco™ system, 40 g gold cartridge, 40 ml flow rate, gradient—0/100 (1 min) to 50/50 (19 min) to 50/50 (21 min—total run time) of EtOAc/hexanes
  12. additionThe fractions containing the product
  13. concentrationconcentrated

出典と根拠

ORDレコード
ord-a768ca25f8bc4002b5a65b7cd1c0aca4
出典データセット
uspto-grants-2016_03
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US09290517B2

反応ノート

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