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Dihydrocholesterol → 3beta-(Prop-2-ynyloxy)cholestanol

HRID 74836
ノート
印刷プレビュー

反応式

HRID 74836 の反応式
[CH3:1][C@@H:2]([C@@H:9]1[C@@:13]2([CH3:28])[CH2:14][CH2:15][C@@H:16]3[C@@:21]4([CH3:27])[CH2:22][CH2:23][C@H:24]([OH:26])[CH2:25][C@@H:20]4[CH2:19][CH2:18][C@H:17]3[C@@H:12]2[CH2:11][CH2:10]1)[CH2:3][CH2:4][CH2:5][CH:6]([CH3:8])[CH3:7].CC(C)([O-:32])C.[K+].[CH2:35](Br)[C:36]#[CH:37]>C1(C)C=CC=CC=1.CCCCCC.CCOC(C)=O>[CH2:35]([O:26][C@H:24]1[CH2:23][CH2:22][C@@:21]2([CH3:27])[CH:20]([CH2:19][CH2:18][C@@H:17]3[C@@H:16]2[CH2:15][CH2:14][C@@:13]2([CH3:28])[C@H:12]3[CH2:11][CH2:10][C@@H:9]2[C@H:2]([CH3:1])[CH2:3][CH2:4][CH2:5][CH:6]([CH3:7])[CH2:8][OH:32])[CH2:25]1)[C:36]#[CH:37]
参加物実験手順後処理出典と根拠反応ノート

参加物

7

反応物 3

HCID 6665DihydrocholesterolHCID 7842Propargyl bromideHCID 23665647Potassium tert-butoxide

生成物 1

HCID 866582823beta-(Prop-2-ynyloxy)cholestanol

試薬・触媒・溶媒 3

HCID 1140Toluene溶媒HCID 8058Hexane溶媒
HCID 8857
Ethyl Acetate
溶媒

実験手順

3β-cholestanol (1.23 g, 3.16 mmol) was completely dissolved in anhydrous toluene (7 mL, 0.45 M) at r.t. Powdered potassium t-butoxide (1.06 g, 9.49 mmol, 3 eq) was added in one portion. The mixture was stirred at r.t. for 3 h. A solution of propargyl bromide (80 wt % in toluene, 0.94 g, 6.32 mmol, 2 eq) was added. The mixture was stirred at r.t. for 3 days. The mixture was diluted with hexane (30 mL) and EtOAc (10 mL), washed with water (2×60 mL) and brine (60 mL). The aqueous phase was extracted once with EtOAc (20 mL). The combined organic phases were dried (Na2SO4), filtered and the filtrate was evaporated onto silica gel and purified by column chromatography (silica gel 2.5×24 cm, gradient elution with hexane 250 mL, hexane-EtOAc 125:5) to give the product as a yellow solid. Recrystallization from EtOAc (3 mL) gave off-white crystals (736 mg, 55%). 1H NMR (CDCl3, 400 MHz) δ 4.18 (d, 2H, J=2.2), 3.45 (m, 1H), 2.38 (t, 1H, J=2.2), 1.99-0.57 (m, 31H), 0.89 (d, 3H, J=6.6), 0.86 (d, 3H, J=6.6), 0.86 (d, 3H, J=6.6), 0.79 (s, 3H), 0.64 (s, 3H).

後処理

  1. stirringThe mixture was stirred at r.t. for 3 days
  2. washwashed with water (2×60 mL) and brine (60 mL)
  3. extractionThe aqueous phase was extracted once with EtOAc (20 mL)
  4. dry with materialThe combined organic phases were dried (Na2SO4)
  5. filtrationfiltered
  6. customthe filtrate was evaporated onto silica gel
  7. custompurified by column chromatography (silica gel 2.5×24 cm, gradient elution with hexane 250 mL, hexane-EtOAc 125:5)

出典と根拠

ORDレコード
ord-217acad05b48403ebec4ecfc19a402bd
出典データセット
uspto-grants-2014_09
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US08828952B2

反応ノート

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