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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 2286818생성일: 2026년 10월 25일

Furfural → Formaldehyde

https://huagongshe.com/reaction/2286818

반응식

참여 물질

역할이름HCID투입량
반응물FurfuralHCID 7362—
반응물1,4-ButanediolHCID 8064—
반응물But-2-yne-1,1-diolHCID 18778928—
생성물FormaldehydeHCID 712—
생성물AcetyleneHCID 6326—
생성물2-Butene-1,4-diolHCID 8065—

반응 단계

Tetrahydrofuran and 1,4-butanediol are both quite useful as organic solvents or as the starting materials for the production of high polymers, and they are manufactured by various processes. For example, it is known that tetrahydrofuran can be produced by the hydrogenation of furan obtained by decarbonylating furfural, or by the dehydrating cyclization of 1,4-butanediol obtainable by hydrogenating either butinediol which can be produced from acetylene and formaldehyde or 2-butene-1,4-diol which can be derived from 1,4-dichlorobutene, or by the hydrogenation of maleic anhydride, or by reacting the acetic ester of 1,4-butanediol with water in the presence of an acidic catalyst. It is also known that 1,4-butanediol can be produced by the hydrogenation of butinediol, or by the hydrolysis of the acetic ester of 1,4-butanediol, or by transesterification reaction of the acetic ester of 1,4-butanediol.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US04268447
출처 데이터셋uspto-grants-1981_05
ORD IDord-bd684d58cc9343e8954e3f2252aae900
출처 메모uspto-grants-1981_05