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Calcium Chloride → (+)-Trans-1-methyl-3-hydroxymethyl-4-(3,4-dichlorophenyl)-piperidine

HRID 227571
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HRID 227571 반응식
[CH3:1][N:2]1[CH2:7][CH2:6][C@H:5]([C:8]2[CH:13]=[CH:12][C:11]([Cl:14])=[C:10]([Cl:15])[CH:9]=2)[C@H:4]([CH2:16][OH:17])[CH2:3]1.CC(C)([O-])C.[K+].[Cl-].[Cl-].[Ca+2]>CN(C)C=O>[CH3:1][N:2]1[CH2:7][CH2:6][C@@H:5]([C:8]2[CH:13]=[CH:12][C:11]([Cl:14])=[C:10]([Cl:15])[CH:9]=2)[C@H:4]([CH2:16][OH:17])[CH2:3]1
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

5

반응물 3

HCID 5284359Calcium ChlorideHCID 9860329HCID 9860329, 화합물HCID 23665647Potassium tert-butoxide

생성물 1

HCID 68533629(+)-Trans-1-methyl-3-hydroxymethyl-4-(3,4-dichlorophenyl)-piperidine

시약·촉매·용매 1

HCID 6228Dimethylformamide용매

실험 절차

A solution of (5) (10.0 g, 36 mmol) and potassium tert-butoxide (12.0 g, 1.08 mmol) in dimethylformamide (75 ml) was stirred over night. CaCl2 (75 ml, 3M) was added and the reaction mixture was extracted with ethyl acetate (2×200 ml). The combined organic phases was dried with sodium sulfate and evaporated to dryness. The residue was recrystallized from ethyl acetate (7 ml). Yield 6.3 g (63%) of (7), mp 137-139° C., [α]D25=+39°.

후처리

  1. extractionthe reaction mixture was extracted with ethyl acetate (2×200 ml)
  2. dry with materialThe combined organic phases was dried with sodium sulfate
  3. customevaporated to dryness
  4. customThe residue was recrystallized from ethyl acetate (7 ml)

출처 및 근거

ORD 기록
ord-f51fadeb3a3a4225b015768e7dcab3c7
출처 데이터셋
uspto-grants-2009_07
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US07560562B2

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