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Water → HCID 11260882、化合物

HRID 1357399
ノート
印刷プレビュー

反応式

HRID 1357399 の反応式
[C:1]([O:4][C:5]([CH3:8])([CH3:7])[CH3:6])(=[O:3])[CH3:2].C([N-]C(C)C)(C)C.[Li+].[O:17]=[C:18]([C@H:24]([CH3:40])[C@@H:25]([O:31][C:32]([O:34][CH2:35][C:36]([Cl:39])([Cl:38])[Cl:37])=[O:33])[C@@H:26]([CH3:30])[CH2:27][CH:28]=[CH2:29])[C:19]([CH3:23])([CH3:22])[CH:20]=[O:21].O>CCOCC.C1COCC1>[O:17]=[C:18]([C@H:24]([CH3:40])[C@@H:25]([O:31][C:32]([O:34][CH2:35][C:36]([Cl:37])([Cl:38])[Cl:39])=[O:33])[C@@H:26]([CH3:30])[CH2:27][CH:28]=[CH2:29])[C:19]([CH3:23])([CH3:22])[C@@H:20]([OH:21])[CH2:2][C:1]([O:4][C:5]([CH3:8])([CH3:7])[CH3:6])=[O:3]
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 962WaterHCID 10908tert-Butyl acetateHCID 2724682Lithium diisopropylamideHCID 11211787(4R,5S,6S)-3-oxo-5-(2,2,2-trichloroethoxycarbonyloxy)-2,2,4,6-tetramethyl-8-nonenal

生成物 1

HCID 11260882HCID 11260882、化合物

試薬・触媒・溶媒 2

HCID 3283
Diethyl Ether
溶媒
3 回
HCID 8028Tetrahydrofuran溶媒

反応条件

温度
-30 °C

実験手順

Tert-butyl acetate (0.865 mL) is added to a solution of lithium diisopropylamide (7.52 mmol) in 30 mL of ether at −78° C., and the mixture is stirred for 1 hour. A solution of bis(1,2:5,6-di-O-isopropylidene-α-L-glucofuranos-3-O-yl)cyclopentadienyltitanium chloride (8.34 mmol) in 90 mL of ether is added dropwise over 40 minutes, and the reaction is stirred for an additional 30 minutes at −78° C., warmed to −30° C. and kept for 45 minutes, then recooled to −78° C. A solution of (4R,5S,6S)-3-oxo-5-(2,2,2-trichloroethoxycarbonyloxy)-2,2,4,6-tetramethyl-8-nonenal (2.57 g) in 15 mL of ether is added over 10 minutes and the reaction is continued for 2 hours before addition of 14 mL of 5 M water in THF. The mix is stirred for 1 hour then filtered through Celite. The filtrate is washed with sat. aq. NaCl, and the brine layer is back extracted with ether. The organic phases are combined, dried with Na2SO4, filtered, and evaporated. The product is purified by chromatography on SiO2 (7% ethyl acetate/hexanes).

後処理

  1. stirringthe reaction is stirred for an additional 30 minutes at −78° C.
  2. waitkept for 45 minutes
  3. customrecooled to −78° C
  4. stirringThe mix is stirred for 1 hour
  5. filtrationthen filtered through Celite
  6. washThe filtrate is washed with sat. aq. NaCl
  7. extractionthe brine layer is back extracted with ether
  8. dry with materialdried with Na2SO4
  9. filtrationfiltered
  10. customevaporated
  11. customThe product is purified by chromatography on SiO2 (7% ethyl acetate/hexanes)

出典と根拠

ORDレコード
ord-52d6a74478b54b3596721e83e44c231b
出典データセット
uspto-grants-2003_07
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US06589968B2

反応ノート

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このページの内容参加物反応条件実験手順後処理出典と根拠反応ノート