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Ammonium Chloride → (R)-oct-7-en-2-ol

HRID 2104228
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HRID 2104228 반응식
[O:1]1[C@H:3]([CH3:4])[CH2:2]1.[CH2:5]([Mg]Br)[CH2:6][CH2:7][CH:8]=[CH2:9].[NH4+].[Cl-]>C1COCC1>[CH3:4][C@@H:3]([OH:1])[CH2:2][CH2:9][CH2:8][CH2:7][CH:6]=[CH2:5]
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참가 물질

5

반응물 3

HCID 25517Ammonium ChlorideHCID 146261(R)-1,2-EpoxypropaneHCID 178445862HCID 178445862, 화합물

생성물 1

HCID 11240489(R)-oct-7-en-2-ol수율 65%

시약·촉매·용매 1

HCID 8028Tetrahydrofuran용매

실험 절차

(R)-(+)-1,2-epoxypropane (1.12 ml, 16.0 mmol) is dissolved in dry THF (23 ml) and CuBr (230 mg, 1.6 mmol) is added therein, after which the temperature is reduced −78° C. The 1M 4-pentenylmagnesium bromide solution (23 ml, 23.5 mmol) prepared in the reaction (1) is added to reaction mixture. The temperature is gradually increased to a room temperature and the mixture is stirred for 4 hours. The reaction is finished with saturated NH4Cl solution (10 ml). An obtained product is extracted with Et2O (20 ml×2) and it is washed by water (10 ml). An organic layer is dried using anhydrous MgSO4. The solution is vacuum concentrated, and then the compound (III) (1.3 g, 65%) is isolated using flash column chromatography (Et2O/n-pentene, 5:1, v/v):

후처리

  1. customis reduced −78° C
  2. additionis added to reaction mixture
  3. extractionAn obtained product is extracted with Et2O (20 ml×2) and it
  4. washis washed by water (10 ml)
  5. customAn organic layer is dried
  6. concentrationconcentrated

출처 및 근거

ORD 기록
ord-be8f98fae195407eb244f88c215bd1aa
출처 데이터셋
uspto-grants-2009_08
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US07576225B2

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