Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
Water → Gamma-Butyrolactone
참여 물질
| 역할 | 이름 | HCID | 투입량 |
|---|---|---|---|
| 반응물 | Water | HCID 962 | — |
| 반응물 | Tetrahydrofuran | HCID 8028 | — |
| 반응물 | 2,5-Dihydrofuran | HCID 15570 | — |
| 촉매 | HCID 178505374 | HCID 178505374 | — |
| 용매 | 1-Butanol | HCID 263 | — |
| 생성물 | Gamma-Butyrolactone | HCID 7302 | — |
| 생성물 | Furan | HCID 8029 | — |
| 생성물 | 2,3-Dihydrofuran | HCID 70934 | — |
| 생성물 | 4-Hydroxybutanal | HCID 93093 | — |
반응 단계
In a manner similar to that described in Example 1, 16 mL/h of 2,5-dihydrofuran and 30 mL/h of water were passed at 230° C. over 253 g of the commercially available copper chromite catalyst marketed by Suedchemie, Munich and bearing the connotation G 22 (composition according to sales brochure: 37% of Cu; 46% of Cr2O3 ; 13% of BaO; reduction in a manner similar to that described in Example 1). At a conversion of 71%, γ-butyrolactone was formed with a selectivity of 67% (2,3-dihydrofuran: 8%; furan: 3%; tetrahydrofuran: 2%; n-butanol: 1%; 4-hydroxybutyraldehyde: 0.5%; remainder: various non-analyzed low-boiling fractions).
출처 및 근거
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| 특허 번호 | US05646307 |
| 출처 데이터셋 | uspto-grants-1997_07 |
| ORD ID | ord-41eba227707c4a7fb38c30d845e22448 |
| 출처 메모 | uspto-grants-1997_07 |