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Methanesulfonic Acid → (3R,4S,5S,6R)-2-(3-(4-((tert-butyldimethylsilyl)oxy)benzyl)-4-chlorophenyl)-6-(hydroxymethyl)-2-methoxytetrahydro-2H-pyran-3,4,5-triol

HRID 628757
ノート
印刷プレビュー

反応式

HRID 628757 の反応式
[Cl:1][C:2]1[CH:22]=[CH:21][C:20](I)=[CH:19][C:3]=1[CH2:4][C:5]1[CH:10]=[CH:9][C:8]([O:11][Si:12]([C:15]([CH3:18])([CH3:17])[CH3:16])([CH3:14])[CH3:13])=[CH:7][CH:6]=1.[CH2:24]([Li])CCC.CCCCCC.C[Si](C)(C)[O:37][C@@H:38]1[C@@H:43]([O:44][Si](C)(C)C)[C@H:42]([O:49][Si](C)(C)C)[C@@H:41]([CH2:54][O:55][Si](C)(C)C)[O:40][C:39]1=[O:60].CS(O)(=O)=O>O1CCCC1.C1(C)C=CC=CC=1.CO>[Si:12]([O:11][C:8]1[CH:9]=[CH:10][C:5]([CH2:4][C:3]2[CH:19]=[C:20]([C:39]3([O:60][CH3:24])[C@H:38]([OH:37])[C@@H:43]([OH:44])[C@H:42]([OH:49])[C@@H:41]([CH2:54][OH:55])[O:40]3)[CH:21]=[CH:22][C:2]=2[Cl:1])=[CH:6][CH:7]=1)([C:15]([CH3:18])([CH3:17])[CH3:16])([CH3:14])[CH3:13]
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

9

反応物 5

HCID 6395Methanesulfonic AcidHCID 8058HexaneHCID 10994280(3R,4S,5R,6R)-3,4,5-Tris-trimethylsilanyloxy-6-trimethylsilanyloxymethyl-tetrahydro-pyran-2-onHCID 1238887024-Iodo-1-chloro-2-[[4-[[(1,1-dimethylethyl)dimethylsilyl]oxy]phenyl]methyl]benzeneHCID 178418339Butyllithium

生成物 1

HCID 123784895
(3R,4S,5S,6R)-2-(3-(4-((tert-butyldimethylsilyl)oxy)benzyl)-4-chlorophenyl)-6-(hydroxymethyl)-2-methoxytetrahydro-2H-pyran-3,4,5-triol

試薬・触媒・溶媒 3

HCID 887Methanol溶媒HCID 1140Toluene溶媒2 回HCID 8028Tetrahydrofuran溶媒

反応条件

温度
-60 °C

実験手順

A solution of (4-(2-chloro-5-iodobenzyl)phenyloxy)tert-butyldimethylsilane (10.0 g, 21.8 mmol) in anhydrous tetrahydrofuran (80 mL) and toluene (80 mL) was cooled to −78° C. To the solution was slowly added dropwise a solution of n-butyl lithium in n-hexane (2.4 mol/L, 13.6 mL, 32.6 mmol). The resulting mixture was reacted at −78° C. for 2 hr, and then warmed up to −60° C. To the reaction mixture was added a solution of (3R,4S,5R,6R)-3,4,5-tri((trimethylsilyl)oxy)-6-(((trimethylsilyl)oxy)methyl)tetra hydro-2H-pyran-2-one (15.3 g, 32.7 mmol) in toluene (60 mL) in one batch. The resulting mixture was reacted at −60° C. for 2 hr. To the reaction mixture was added dropwise a solution of methanesulfonic acid (14.6 g, 152.1 mmol) in methanol (50 mL). After the completion of dropwise addition, the resulting mixture was reacted under stirring at room temperature for 17 hr. The reaction mixture was quenched with a saturated sodium bicarbonate solution, and separated into an aqueous phase and an organic phase. The aqueous phase was extracted with ethyl acetate (200 mL×3). The organic phases were combined, washed with a saturated sodium chloride solution, dried over anhydrous sodium sulphate, and concentrated under a reduced pressure to produce 9.0 g of a crude product, which was directly used in the next reaction without purification.

後処理

  1. customThe resulting mixture was reacted at −78° C. for 2 hr
  2. customThe resulting mixture was reacted at −60° C. for 2 hr
  3. additionAfter the completion of dropwise addition
  4. customthe resulting mixture was reacted
  5. customThe reaction mixture was quenched with a saturated sodium bicarbonate solution
  6. customseparated into an aqueous phase
  7. extractionThe aqueous phase was extracted with ethyl acetate (200 mL×3)
  8. washwashed with a saturated sodium chloride solution
  9. dry with materialdried over anhydrous sodium sulphate
  10. concentrationconcentrated under a reduced pressure

出典と根拠

ORDレコード
ord-837d3f798add4578a823c9e297008dae
出典データセット
uspto-grants-2016_04
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US09315438B2

反応ノート

読み込み中…

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