참여 물질
| 역할 | 이름 | HCID | 투입량 |
|---|
| 반응물 | Butylated Hydroxyanisole | HCID 8456 | — |
| 반응물 | HCID 131715859 | HCID 131715859 | — |
| 생성물 | HCID 137331181 | HCID 137331181 | — |
반응 단계
Para-aminophenol is acetylated by reaction with acetic anhydride to form 4-acetoxyacetanilide, which is then nitrated to form 4-acetoxy-2-nitroacetanilide (V). V is then reacted with 3-chloropropyldimethylvinylsilane to form 4-(3'-dimethylvinylsilylpropoxy)-2-nitroacetanilide (VI). VI is hydrolyzed to form VII, which is then reacted with nitrous acid to form a 4-(3'-dimethylvinylsilylpropoxy)-2-nitrobenzenediazonium ion (VIII). The diazonium ion VIII is then reacted with 2-t-butyl-4-methoxyphenol to form 2-t-butyl-6-[4'-(3"-dimethylvinylsilylpropoxy)-2'-nitrophenylazo]-4-methoxyphenol (IX). The azo compound IX is then reacted with glucose and base, and then with zinc to form 2-(3'-t-butyl-2'-hydroxy-5'-methoxyphenyl)-5-(3"-dimethyl-vinylsilylpropoxy)benezotriazole (X).
출처 및 근거
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|
| 특허 번호 | US04803254 |
|---|
| 출처 데이터셋 | uspto-grants-1989_02 |
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| ORD ID | ord-4a1d7314514445ada68edccabd737529 |
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| 출처 메모 | uspto-grants-1989_02 |
|---|