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Water → 10-Iodo-9-decenoate methyl ester

HRID 521756
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HRID 521756 반응식
[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]
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참가 물질

7

반응물 3

HCID 962WaterHCID 6374IodoformHCID 14133290(E)-methyl 10-iododec-9-enoate

생성물 1

HCID 7272788410-Iodo-9-decenoate methyl ester수율 63%

시약·촉매·용매 3

HCID 3283Diethyl Ether용매HCID 8028Tetrahydrofuran용매
HCID 31275
1,4-Dioxane
용매

실험 절차

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.

후처리

  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)

출처 및 근거

ORD 기록
ord-964fa0171cec4483b8709475ac80cf96
출처 데이터셋
uspto-grants-2016_05
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US09328127B2

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