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Water → 10-Iodo-9-decenoate methyl ester

HRID 521756
ノート
印刷プレビュー

反応式

HRID 521756 の反応式
[I:1]/[CH:2]=[CH:3]/[CH2:4][CH2:5][CH2:6][CH2:7][CH2:8][CH2:9][CH2:10][C:11]([O:13][CH3:14])=[O:12].C(I)(I)I.O>C1COCC1.O1CCOCC1.CCOCC>[CH3:14][O:13][C:11](=[O:12])[CH2:10][CH2:9][CH2:8][CH2:7][CH2:6][CH2:5][CH2:4][CH:3]=[CH:2][I:1]
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 962WaterHCID 6374IodoformHCID 14133290(E)-methyl 10-iododec-9-enoate

生成物 1

HCID 7272788410-Iodo-9-decenoate methyl ester収率 63%

試薬・触媒・溶媒 3

HCID 3283Diethyl Ether溶媒HCID 8028Tetrahydrofuran溶媒
HCID 31275
1,4-Dioxane
溶媒

実験手順

To a suspension of CrCl2 (454 mg, 3.75 mmol, 7.0 eq.) in THF (1.5 mL) at 23° C. was added dropwise a solution of (E)-methyl 10-iododec-9-enoate (100 mg, 0.537 mmol, 1.0 eq.) and iodoform (422 mg, 1.07 mmol, 2.0 eq.) in dioxane (9.2 mL). After stirring for 12 h, the reaction mixture was diluted with Et2O (10 mL) and poured into water (10 mL). The layers were separated and the aqueous layer was extracted with Et2O (3×15 mL). The combined organic extracts were washed with brine (10 mL), dried over MgSO4, and concentrated in vacuo. Purification of the crude product by flash chromatography (hexanes→hexanes:EtOAc 9:1) provided 10-iodo-9-decenoate methyl ester as a yellow oil (105 mg, 0.337 mmol, 63%). 1H NMR indicated an E:Z ratio of 10:1.

後処理

  1. customThe layers were separated
  2. extractionthe aqueous layer was extracted with Et2O (3×15 mL)
  3. washThe combined organic extracts were washed with brine (10 mL)
  4. dry with materialdried over MgSO4
  5. concentrationconcentrated in vacuo
  6. customPurification of the crude product by flash chromatography (hexanes→hexanes:EtOAc 9:1)

出典と根拠

ORDレコード
ord-964fa0171cec4483b8709475ac80cf96
出典データセット
uspto-grants-2016_05
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US09328127B2

反応ノート

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