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Imidazole → tert-butyl (3R)-3-(iodomethyl)pyrrolidine-1-carboxylate

HRID 927983
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HRID 927983 반응식
[I:1]I.N1C=CN=C1.C1(P(C2C=CC=CC=2)C2C=CC=CC=2)C=CC=CC=1.O[CH2:28][C@@H:29]1[CH2:33][CH2:32][N:31]([C:34]([O:36][C:37]([CH3:40])([CH3:39])[CH3:38])=[O:35])[CH2:30]1>C(OCC)C.O1CCOCC1>[I:1][CH2:28][C@@H:29]1[CH2:33][CH2:32][N:31]([C:34]([O:36][C:37]([CH3:40])([CH3:39])[CH3:38])=[O:35])[CH2:30]1
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참가 물질

7

반응물 4

HCID 795ImidazoleHCID 807IodineHCID 11776TriphenylphosphineHCID 1514340tert-Butyl (3R)-3-(hydroxymethyl)pyrrolidine-1-carboxylate

생성물 1

HCID 59371368tert-butyl (3R)-3-(iodomethyl)pyrrolidine-1-carboxylate수율 93.1%

시약·촉매·용매 2

HCID 3283
Diethyl Ether
용매
2회
HCID 312751,4-Dioxane용매

실험 절차

Iodine (1.91 g) was added in portions to a vigorously stirred, ice cooled suspension of imidazole (0.681 g) and triphenylphosphine (1.97 g) in diethyl ether (12 mL). The mixture was then stirred for 10 minutes before a solution of tert butyl (R)-3-hydroxymethylpyrrolidine-1-carboxylate (1 g) in dioxane (6 mL) was added dropwise. The resulting mixture was stirred at room temperature overnight, then diluted with diethyl ether and filtered. The solid was washed with diethyl ether and the combined filtrate was evaporated to dryness. The residue was purified by chromatography on silica, eluting with a mixture of ethyl acetate and pentane with a gradient of 0-20% to give tert-butyl (R)-3-iodomethylpyrrolidine-1-carboxylate (1.44 g) as an oil.

후처리

  1. temperatureice cooled
  2. additionwas added dropwise
  3. stirringThe resulting mixture was stirred at room temperature overnight
  4. filtrationfiltered
  5. washThe solid was washed with diethyl ether
  6. customthe combined filtrate was evaporated to dryness
  7. customThe residue was purified by chromatography on silica
  8. washeluting with a mixture of ethyl acetate and pentane with a gradient of 0-20%

출처 및 근거

ORD 기록
ord-a1aee225980442869f46cc6d9fe4f392
출처 데이터셋
uspto-grants-2016_03
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US09290472B2

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