GB190501202A - Improvements in the Manufacture of Non-inflammable Products from Benzene - Google Patents

Improvements in the Manufacture of Non-inflammable Products from Benzene

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Publication number
GB190501202A
GB190501202A GB190501202DA GB190501202A GB 190501202 A GB190501202 A GB 190501202A GB 190501202D A GB190501202D A GB 190501202DA GB 190501202 A GB190501202 A GB 190501202A
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United Kingdom
Prior art keywords
benzene
vessel
iodine
chlorine
condenser
Prior art date
Legal status (The legal status is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the status listed.)
Expired
Application number
Inventor
Henry Birkbeck
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Individual
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Individual
Priority date (The priority date is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the date listed.)
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Publication date
Application filed by Individual filed Critical Individual
Application granted granted Critical
Publication of GB190501202A publication Critical patent/GB190501202A/en
Expired legal-status Critical Current

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  • Inorganic Compounds Of Heavy Metals (AREA)
  • Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)

Abstract

1202. Birkbeck, H., [Barboni, E. B.]. Jan. 21. Chloro-benzenes.-Benzene is chlorinated in the presence of carbon bisulphide and iodine, or substances such as antimony, pentachloride, for the purpose of rendering it non-inflammable. The benzene is contained in an enamelled cast-iron vessel A, provided with a water jacket B, or an internal steam coil, and with a hollow perforated rotating stirrer C, through which dry chlorine is introduced. The vessel A is connected with either a reflux condenser D or an ordinary condenser H, as may be required. In the example given, benzene is mixed with carbon bisulphide, and iodine is dissolved in the mixture. Chlorine is introduced, with stirring, the vessel being connected with the reflux condenser, and the hydrochloric acid evolved being absurbed in water in the carboys F. Suction may be applied at G. The operation ceases when iodine chloride is deposited. Sulphur is then added to the cooled liquid through a man-hole, the current of chlorine being interrupted. The vessel being connected with the condenser H, a jet of steam is introduced into the jacket, and the liquid is distilled. The distillate is agitated with water to decompose sulphur chloride, decanted, and agitated with dilute caustic soda, after which the product is dried, e.g. with calcium chloride, and then filtered. The product is a mixture of chluro derivatives dissolved in unchanged benzene, their general formula being C6 H6-n Cln Specification No. 17,695, A.D. 1902, is referred to.
GB190501202D 1905-01-21 1905-01-21 Improvements in the Manufacture of Non-inflammable Products from Benzene Expired GB190501202A (en)

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
GB190501202T 1905-01-21

Publications (1)

Publication Number Publication Date
GB190501202A true GB190501202A (en) 1906-01-18

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ID=32193170

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GB190501202D Expired GB190501202A (en) 1905-01-21 1905-01-21 Improvements in the Manufacture of Non-inflammable Products from Benzene

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GB (1) GB190501202A (en)

Cited By (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US3226447A (en) * 1960-12-22 1965-12-28 Union Carbide Australia Directed nuclear substitution-chlorination of aromatic hydrocarbons and halogenated aromatic hydrocarbons

Cited By (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US3226447A (en) * 1960-12-22 1965-12-28 Union Carbide Australia Directed nuclear substitution-chlorination of aromatic hydrocarbons and halogenated aromatic hydrocarbons

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