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llms.txt · MCP 가이드개인정보처리방침 · 이용약관 · 지원v1.8.0
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Ammonium Chloride → HCID 131727207, 화합물

HRID 1698381
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HRID 1698381 반응식
[CH:1]1([Mg]Cl)[CH2:6][CH2:5][CH2:4][CH2:3][CH2:2]1.[CH3:9][Si:10]([O:13][CH3:14])(Cl)Cl.[Cl-].[NH4+]>C1COCC1>[CH:1]1([CH:9]([SiH2:10][O:13][CH3:14])[CH:1]2[CH2:6][CH2:5][CH2:4][CH2:3][CH2:2]2)[CH2:6][CH2:5][CH2:4][CH2:3][CH2:2]1
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참가 물질

5

반응물 3

HCID 25517Ammonium ChlorideHCID 74580DichloromethoxymethylsilaneHCID 178478990HCID 178478990, 화합물

생성물 1

HCID 131727207HCID 131727207, 화합물수율 80%

시약·촉매·용매 1

HCID 8028Tetrahydrofuran용매

실험 절차

The THF solution of cyclohexyl magnesium chloride as prepared above was added dropwise to the methylmethoxydichlorosilane solution obtained in Example 7, in the same manner as in Example 3(c), to effect the Grignard reaction. The post-treatment of the resulting Grignard reaction solution was carried out in the same manner as in Example 3(c), except that the saturated aqueous ammonium chloride solution used in Example 3(c), was used in a reduced amount of 80 ml instead of 120 ml. The organic layer was separated and was fractionally distilled under a reduced pressure, thereby to afford 39 g of dicyclohexylmethylmethoxysilane as a fraction boiling at 128° C.-129° C./7 mm Hg (yield; 80%).

후처리

  1. customthe Grignard reaction
  2. customThe post-treatment of the resulting Grignard reaction solution
  3. customThe organic layer was separated
  4. distillationwas fractionally distilled under a reduced pressure

출처 및 근거

ORD 기록
ord-df7a0f79ca5148299bd5758d25785260
출처 데이터셋
uspto-grants-2012_04
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US08163950B2

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