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Acetylene → Androst-16-ene

HRID 1081518
ノート
印刷プレビュー

反応式

HRID 1081518 の反応式
[CH2:1]([Li])[CH2:2][CH2:3][CH3:4].C#C.I[CH2:9][CH2:10][CH2:11][CH2:12][CH2:13][CH2:14][CH2:15][CH2:16][CH2:17][CH2:18]I.[CH3:20][CH2:21][CH2:22][CH2:23][CH2:24]C>O1CCCC1>[CH3:4][C@:3]12[CH2:24][CH2:23][C@H:22]3[C@@H:11]([CH2:12][CH2:13][CH:14]4[C@:21]3([CH3:20])[CH2:18][CH2:17][CH2:16][CH2:15]4)[C@@H:10]1[CH2:9][CH:1]=[CH:2]2
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 4

HCID 6326AcetyleneHCID 8058HexaneHCID 853781,10-DiiododecaneHCID 178418339Butyllithium

生成物 1

HCID 161178Androst-16-ene収率 26%

試薬・触媒・溶媒 1

HCID 8028Tetrahydrofuran溶媒3 回

反応条件

温度
-10 °C

実験手順

To a solution of butyllithium (2.84 ml of a 1.6 M solution in hexane, 4.5 mmol) in dry tetrahydrofuran (THF, 45 ml) was added dropwise a solution of acetylene 9 (500 mg, 1.13 mmol) in dry THF (10 ml) at -40° C. The reaction mixture was then allowed to warm up to -10° C. and stirred for 1 h. At his temperature, a solution of 1,10-diiododecan (2.15 g, 5.4 mmol) in dry THF (5 ml) was added in one portion. The cooling bath was removed and the reaction mixture was stirred at room temperature for 15 h. Then, the solution was diluted with 100 ml of ether and was washed with water (6×30 ml), dried, filtered and concentrated to an oil. The residue was purified by flash chromatography (hexane:acetone, 96:4), followed by preparative thin-layer chromatography (TLC) to give 208 mg, 26% of compound 10 (n=10)

後処理

  1. customThe cooling bath was removed
  2. stirringthe reaction mixture was stirred at room temperature for 15 h
  3. additionThen, the solution was diluted with 100 ml of ether
  4. washwas washed with water (6×30 ml)
  5. customdried
  6. filtrationfiltered
  7. concentrationconcentrated to an oil
  8. customThe residue was purified by flash chromatography (hexane:acetone, 96:4)

出典と根拠

ORDレコード
ord-44298cb65d994fa1a1270ab55f2ce1e8
出典データセット
uspto-grants-1996_12
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US05585405

反応ノート

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