Benzylamine → HCID 54426674, 화합물

HRID 865993노트

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HRID 865993 반응식
[O:1]1[CH2:20][CH:2]1[CH2:3][O:4][CH2:5][CH2:6][CH2:7][Si:8]([CH3:19])([O:14][Si:15]([CH3:18])([CH3:17])[CH3:16])[O:9][Si:10]([CH3:13])([CH3:12])[CH3:11].[CH2:21]([NH2:28])[C:22]1[CH:27]=[CH:26][CH:25]=[CH:24][CH:23]=1>C(O)(C)C>[CH2:21]([NH:28][CH2:20][CH:2]([OH:1])[CH2:3][O:4][CH2:5][CH2:6][CH2:7][Si:8]([CH3:19])([O:14][Si:15]([CH3:18])([CH3:17])[CH3:16])[O:9][Si:10]([CH3:13])([CH3:12])[CH3:11])[C:22]1[CH:27]=[CH:26][CH:25]=[CH:24][CH:23]=1

참가 물질

4

반응물 2

HCID 7504BenzylamineHCID 62635Trisiloxane, 1,1,1,3,5,5,5-heptamethyl-3-(3-(2-oxiranylmethoxy)propyl)-2회

생성물 1

HCID 54426674HCID 54426674, 화합물

시약·촉매·용매 1

HCID 3776Isopropanol용매2회

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온도
80 °C

실험 절차

A 500-ml, three-necked, round-bottomed flask equipped with a stirrer, addition funnel, and condenser was charged with 100 g (0.30 mole) of the epoxy trisiloxane (Compound I) of Example 1 dissolved in 200 ml of isopropanol. The addition funnel was charged with a solution of 42.8 g (0.4 mole) of benzylamine (Aldrich) in 100 ml of isopropanol the solution was added drop-wise to the flask contents at room temperature. The resulting reaction solution was heated at 80° C. for eight hours, after which time the solvent was removed under reduced pressure using a rotary evaporator. The residue, an oil, was passed through a short silica column using 10% ethyl acetate in hexane as eluent. The yield of Compound V, a colorless oil, was 127.8 g (979). The following elemental analysis was obtained:

후처리

  1. customA 500-ml, three-necked, round-bottomed flask equipped with a stirrer, addition funnel, and condenser
  2. additionwas added drop-wise to the flask contents at room temperature
  3. customThe resulting reaction solution
  4. customafter which time the solvent was removed under reduced pressure
  5. customa rotary evaporator
  6. customThe following elemental analysis was obtained

출처 및 근거

ORD 기록
ord-8552c6d0e76a455dadf30253a49308f9
출처 데이터셋
uspto-grants-1996_10
특허 번호
US05569732

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