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Tetrahydrofuran → HCID 71520078、化合物

HRID 633664
ノート
印刷プレビュー

反応式

HRID 633664 の反応式
C1COCC1.[CH3:6][O:7][C:8]1[C@:15]2([CH2:18][CH:19]=[C:20]([CH3:22])[CH3:21])[C:16](=[O:17])[C@@H:11]([C@:12]([CH3:42])([CH2:28][CH2:29][CH2:30][C:31]([CH3:41])([O:33][Si:34]([CH2:39][CH3:40])([CH2:37][CH3:38])[CH2:35][CH3:36])[CH3:32])[C@@H:13]([CH2:23][CH:24]=[C:25]([CH3:27])[CH3:26])[CH2:14]2)[C:10](=[O:43])[C:9]=1[Si:44]([CH3:47])([CH3:46])[CH3:45].[Li]N1C(C)(C)CCCC1(C)C.[C:59](Cl)(=[O:63])[CH:60]([CH3:62])[CH3:61]>CCOC(C)=O.CCCCCC>[C:59]([C@:11]12[C:16](=[O:17])[C@:15]([CH2:18][CH:19]=[C:20]([CH3:21])[CH3:22])([CH2:14][C@H:13]([CH2:23][CH:24]=[C:25]([CH3:27])[CH3:26])[C@@:12]1([CH3:42])[CH2:28][CH2:29][CH2:30][C:31]([CH3:41])([O:33][Si:34]([CH2:35][CH3:36])([CH2:37][CH3:38])[CH2:39][CH3:40])[CH3:32])[C:8]([O:7][CH3:6])=[C:9]([Si:44]([CH3:47])([CH3:46])[CH3:45])[C:10]2=[O:43])(=[O:63])[CH:60]([CH3:62])[CH3:61]
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 8028Tetrahydrofuran2 回HCID 62325Isobutyryl chlorideHCID 71520077HCID 71520077、化合物2 回HCID 178418821HCID 178418821、化合物

生成物 1

HCID 71520078HCID 71520078、化合物収率 24%

試薬・触媒・溶媒 2

HCID 8058
Hexane
溶媒
HCID 8857Ethyl Acetate溶媒

反応条件

温度
0 °C

実験手順

A THF (0.5 mL) solution of 45 (7.0 mg, 11 μmol, 1 equiv.) was cooled to −78° C. in a 10-mL test tube, and a freshly prepared THF solution of lithium tetramethylpiperidide (0.50 M, 113 μL, 57 μmol, 5 equiv.) was added dropwise. The resulting yellow-orange solution was stirred at −78° C. for 10 min and at 0° C. for 10 min. The solution was then cooled to −78° C., and isobutyryl chloride (6.0 μL, 57 μmol, 5 equiv.) was added. The resulting yellow solution was stirred at −78° C. for 50 min, was slowly warmed to 0° C. over 50 min, and subsequently quenched with saturated aqueous NaHCO3. The mixture was warmed to room temperature and extracted thrice with EtOAc. The organic extracts were combined, washed with H2O and brine, dried over Na2SO4, filtered, and concentrated in vacuo to a yellow residue. Preparatory thin-layer chromatography (3×98:2 hexane:EtOAc) afforded 1.8 mg (2.6 μmol, 24% yield) of 46 as a colorless residue along with 1.7 mg (2.8 μmol, 25% recovery) of 45. TLC Rf 0.47 (95:5 hexane:EtOAc). 1H-NMR (600 MHz; CDCl3): δ 5.00-4.96 (m, 2H), 3.90 (s, 3H), 2.55 (dd, J=14.6, 6.4 Hz, 1H), 2.41 (dd, J=14.5, 7.7 Hz, 1H), 2.08 (d, J=15.0 Hz, 1H), 1.97 (septet, J=6.5 Hz, 1H), 1.92-1.85 (m, 2H), 1.79-1.72 (m, 1H), 1.68 (s, 3H), 1.66 (s, 3H), 1.57-1.56 (m, 3H), 1.55-1.53 (m, 3H), 1.50-1.42 (m, 2H), 1.39-1.31 (m, 3H), 1.30-1.24 (m, 2H), 1.17 (s, 3H), 1.17 (s, 3H), 1.13 (d, J=6.5 Hz, 3H), 1.02 (d, J=6.5 Hz, 3H), 0.98 (s, 3H), 0.92 (t, J=7.9 Hz, 9H), 0.54 (q, J=7.9 Hz, 6H), 0.26 (s, 9H). HRMS-ESI (m/z): [M+Na]+ calculated for C40H70O5Si2, 709.4654. found, 709.4626.

後処理

  1. temperatureThe solution was then cooled to −78° C.
  2. stirringThe resulting yellow solution was stirred at −78° C. for 50 min
  3. temperaturewas slowly warmed to 0° C. over 50 min
  4. customsubsequently quenched with saturated aqueous NaHCO3
  5. temperatureThe mixture was warmed to room temperature
  6. extractionextracted thrice with EtOAc
  7. washwashed with H2O and brine
  8. dry with materialdried over Na2SO4
  9. filtrationfiltered
  10. concentrationconcentrated in vacuo to a yellow residue

出典と根拠

ORDレコード
ord-f4827c153cc94f78843a58d871301d5f
出典データセット
uspto-grants-2016_04
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US09321713B2

反応ノート

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