홈MCP워크벤치Skills
홈워크벤치알림마이페이지
llms.txt · MCP 가이드개인정보처리방침 · 이용약관 · 지원v1.8.0
  1. 홈
  2. /반응

Ammonia → (3-Aminopropyl)triethoxysilane

HRID 224739
노트
인쇄 미리보기

반응식

HRID 224739 반응식
[NH3:1].[Cl:2][CH2:3][CH2:4][CH2:5][Si:6]([O:13][CH2:14][CH3:15])([O:10][CH2:11][CH3:12])[O:7][CH2:8][CH3:9]>>[Cl:2][CH2:3][CH2:4][CH2:5][Si:6]([O:13][CH2:14][CH3:15])([O:7][CH2:8][CH3:9])[O:10][CH2:11][CH3:12].[NH2:1][CH2:3][CH2:4][CH2:5][Si:6]([O:13][CH2:14][CH3:15])([O:10][CH2:11][CH3:12])[O:7][CH2:8][CH3:9]
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

4

반응물 2

HCID 222Ammonia2회HCID 78771(3-Chloropropyl)triethoxysilane

생성물 2

HCID 13521(3-Aminopropyl)triethoxysilaneHCID 78771(3-Chloropropyl)triethoxysilane

실험 절차

Into a ten-liter steel autoclave with stirrer, 3400 g (200 moles) of liquid ammonia was poured, and the reactor was sealed. Then the ammonia was heated to 75° C., causing a pressure of 36 bars to be established. After this temperature was reached, γ-chloropropyltriethoxysilane was fed in, with stirring at 183 rpm, for a period of one hour, in the amount of 2.67 moles; then stirring was continued for 8 hours at 75° C. Then the pressure was let off and the ammonia was removed. After the removal of ammonium chloride by filtration, the remaining raw product was purified by vacuum distillation. From the 642 grams of γ-chloropropyltriethoxysilane, 486 g of γ-aminopropyltriethoxysilane was obtained (82.4% of the theoretical yield) plus 98.3 g of byproducts (secondary and tertiary amines).

후처리

  1. customthe reactor was sealed
  2. stirringthen stirring
  3. waitwas continued for 8 hours at 75° C
  4. customthe ammonia was removed
  5. customAfter the removal of ammonium chloride
  6. filtrationby filtration
  7. distillationthe remaining raw product was purified by vacuum distillation

출처 및 근거

ORD 기록
ord-be521702e17b4bb5967e091e186e04e9
출처 데이터셋
uspto-grants-1980_11
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US04234502

반응 노트

불러오는 중…

이 페이지에서참가 물질실험 절차후처리출처 및 근거반응 노트