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N-Methyloctadecylamine → HCID 21482430, 화합물

HRID 1415445
노트
인쇄 미리보기

반응식

HRID 1415445 반응식
Br[CH2:2][CH2:3][CH2:4][Si:5]([O:10][CH3:11])([O:8][CH3:9])[O:6][CH3:7].[CH2:12]([NH:30]C)[CH2:13][CH2:14][CH2:15][CH2:16][CH2:17][CH2:18][CH2:19][CH2:20][CH2:21][CH2:22][CH2:23][CH2:24][CH2:25][CH2:26][CH2:27][CH2:28][CH3:29].[O-][CH2:33]C.[Na+]>C(O)C>[CH3:33][CH:14]([CH2:15][CH2:16][CH2:17][CH2:18][CH2:19][CH2:20][CH2:21][CH2:22][CH2:23][CH2:24][CH2:25][CH2:26][CH2:27][CH2:28][CH3:29])[CH2:13][CH2:12][NH:30][CH2:2][CH2:3][CH2:4][Si:5]([O:10][CH3:11])([O:8][CH3:9])[O:6][CH3:7]
참가 물질반응 조건실험 절차후처리출처 및 근거반응 노트

참가 물질

5

반응물 3

HCID 75539N-MethyloctadecylamineHCID 103984(3-Bromopropyl)trimethoxysilaneHCID 2723922Sodium ethoxide

생성물 1

HCID 21482430HCID 21482430, 화합물

시약·촉매·용매 1

HCID 702Ethanol용매2회

반응 조건

온도
103.5 °C

실험 절차

A mixture of 12.0g of gamma-bromopropyltrimethoxysilane and 14.15g of octadecylmethylamine are heated at 94-113° C. for 16 hours and then cooled. The resulting tertiary ammonium salt is dissolved in 100 ml of absolute ethanol and 0.05 moles of freshly prepared sodium ethoxide in 50 ml of ethanol is added. Filtration of the resulting solution and removal of the solvent yield the tertiary amine, gammamethyloctadecylaminopropyltrimethoxysilane.

후처리

  1. temperaturecooled
  2. filtrationFiltration of the resulting solution and removal of the solvent

출처 및 근거

ORD 기록
ord-91f4f54af69d49239773de286b5d2d64
출처 데이터셋
uspto-grants-1977_01
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US04005119

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