참여 물질
| 역할 | 이름 | HCID | 투입량 |
|---|
| 반응물 | 1-Naphthol | HCID 7005 | — |
| 반응물 | 1-Hexanol | HCID 8103 | — |
| 반응물 | Isobutylene | HCID 8255 | — |
| 반응물 | Di-tert-butyl ether | HCID 22541 | — |
| 반응물 | Hexyl t-butyl ether | HCID 547839 | — |
| 생성물 | 1-(tert-Butoxy)naphthalene | HCID 170831 | 67% |
반응 단계
The influence on the acid-catalyzed formation of t-butyl ether from isobutene with n-hexanol and 1-naphthol was examined in a competitive reaction. The formation of dimers and oligomers of isobutene as side-products was to be suppressed, and selectivity for one of the two alcohols was to be achieved. While the formation of almost 25% of isobutene dimers, based on the ethers formed, occurs in methyl-free Sn-containing Si glass (3% Sn, 97% Si), no dimer formation can be detected in the product with methyl-containing Sn--Si glass (30% Me--Si, 3% Sn, 67% Si). With methyl-free Al-containing Si glass (3% Al, 97% Si), the formation of isobutene dimers predominates, and the yield is around 67% naphthol t-butyl ether and 37% n-hexyl t-butyl ether. With methyl-containing Al-Si glass (10% Me--Si, 3% Al, 87% Si), only 30% isobutene dimers form, relatively to the ether formation, and the yield of ethers increases to 57% n-hexyl t-butyl ether and 43% naphthol t-butyl ether. This suppression of dimer formation and change of the ether selectivity with increasing methyl content of the glasses is continued in Zr-containing glasses.
출처 및 근거
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| 특허 번호 | US06121187 |
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| 출처 데이터셋 | uspto-grants-2000_09 |
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| ORD ID | ord-275d8bccfe8e4bcfaab816cf763f7d62 |
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| 출처 메모 | uspto-grants-2000_09 |
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