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Ethylene Oxide → 2-[(3R)-3-methoxymethylmorpholino]ethanol

HRID 1374976
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HRID 1374976 반응식
Cl.[CH3:2][O:3][CH2:4][C@@H:5]1[CH2:10][O:9][CH2:8][CH2:7][NH:6]1.C(N(CC)CC)C.[CH2:18]1[O:20][CH2:19]1>CO.C1(C)C=CC=CC=1>[CH3:2][O:3][CH2:4][C@H:5]1[N:6]([CH2:18][CH2:19][OH:20])[CH2:7][CH2:8][O:9][CH2:10]1
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

6

반응물 3

HCID 6354Ethylene OxideHCID 8471TriethylamineHCID 53338712(3R)-3-(Methoxymethyl)morpholine--hydrogen chloride (1/1)

생성물 1

HCID 538274862-[(3R)-3-methoxymethylmorpholino]ethanol

시약·촉매·용매 2

HCID 887Methanol용매HCID 1140Toluene용매

실험 절차

이 페이지에서참가 물질실험 절차후처리출처 및 근거반응 노트

To a mixed solution of (3R)-3-(methoxymethyl)morpholine hydrochloride (4.71 g) and triethylamine (4.11 ml) in methanol (110 ml) was added 5.8M ethylene oxide (22 ml) in toluene solution at room temperature. After the reaction mixture was stirred at the same temperature for two days, it was evaporated under reduced pressure. The residue was purified by column chromatography on silica gel using mixed solvents of dichloromethane and methanol (20:1). The fractions containing the objective compound were collected and evaporated under reduced pressure to give 2-[(3R)-3-methoxymethylmorpholino]ethanol (4.67 g) as an oil.

후처리

  1. customit was evaporated under reduced pressure
  2. customThe residue was purified by column chromatography on silica gel using
  3. additionmixed solvents of dichloromethane and methanol (20:1)
  4. additionThe fractions containing the objective compound
  5. customwere collected
  6. customevaporated under reduced pressure

출처 및 근거

ORD 기록
ord-8b950683a79e4a3fbb2937c07e4313a1
출처 데이터셋
uspto-grants-2007_01
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US07166598B2

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