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HRID 46751作成日:2026年10月24日

Sulfuric Acid → Hexachlorobutadiene

https://huagongshe.com/ja/reaction/46751

反応式

関与物質

役割名称HCID仕込み量
反応物Sulfuric AcidHCID 1118—
反応物2,3,4,4-Tetrachloro-2-cyclobuten-1-oneHCID 18545—
反応物HexachlorocyclobuteneHCID 22504—
反応物Sulfur trioxideHCID 24682—
生成物HexachlorobutadieneHCID 6901—
生成物HexachlorocyclobuteneHCID 22504—

反応手順

Tetrachlorocyclobutenone, required as a starting material, is obtained with high yields and conversions by a not yet published process from hexachlorocyclobutene and a mixture of sulphuric acid and sulphur trioxide at elevated temperatures, e.g., by reaction of 1 mol hexachlorocyclobutene with approximately 1 mol each of sulphuric acid and sulphur trioxide at a temperature of 80° C. within 5 hours. Hexachlorocyclobutene can be obtained from hexachloro-1,3-butadiene in yields of near 100% of theory (DE-OS No. 26 18 557), corresponding to U.S. Pat. No. 4,115,460), for example by rectifying commercial hexachlorobutadiene at a pressure of from 2 to 100 mm Hg with a reflux ratio of from 300:1 to 600:1, subjecting hexachlorobutadiene remaining in the bottoms to a heat treatment at from 150° to 200° C. and then returning it to the rectifying column together with fresh commercial hexachlorobutadiene while withdrawing the product rich in hexachlorocyclobutene over the top. A suitable starting material is not only pure tetrachlorocyclobutenone but also crude tetrachlorocyclobutenone which may, for example, contain hexachlorobutadiene and hexachlorocyclobutene originating from its process of manufacture.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US04175095
出典データセットuspto-grants-1979_11
ORD IDord-836302dff01f4cb2b1919c94896ee549
出典メモuspto-grants-1979_11