GB738171A - Process for the preparation of propylene chlorhydrin - Google Patents

Process for the preparation of propylene chlorhydrin

Info

Publication number
GB738171A
GB738171A GB2712752A GB2712752A GB738171A GB 738171 A GB738171 A GB 738171A GB 2712752 A GB2712752 A GB 2712752A GB 2712752 A GB2712752 A GB 2712752A GB 738171 A GB738171 A GB 738171A
Authority
GB
United Kingdom
Prior art keywords
propylene
chlorine
chlorhydrin
solution
zone
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
GB2712752A
Inventor
Paul Ferrero
Leon Rene Flamme
Michel Fourez
Current Assignee (The listed assignees may be inaccurate. Google has not performed a legal analysis and makes no representation or warranty as to the accuracy of the list.)
CARBOCHIMIQUE SA
Original Assignee
CARBOCHIMIQUE SA
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.)
Filing date
Publication date
Application filed by CARBOCHIMIQUE SA filed Critical CARBOCHIMIQUE SA
Priority to GB2712752A priority Critical patent/GB738171A/en
Publication of GB738171A publication Critical patent/GB738171A/en
Expired legal-status Critical Current

Links

Classifications

    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07CACYCLIC OR CARBOCYCLIC COMPOUNDS
    • C07C29/00Preparation of compounds having hydroxy or O-metal groups bound to a carbon atom not belonging to a six-membered aromatic ring
    • C07C29/64Preparation of compounds having hydroxy or O-metal groups bound to a carbon atom not belonging to a six-membered aromatic ring by simultaneous introduction of -OH groups and halogens
    • C07C29/66Preparation of compounds having hydroxy or O-metal groups bound to a carbon atom not belonging to a six-membered aromatic ring by simultaneous introduction of -OH groups and halogens by addition of hypohalogenous acids, which may be formed in situ, to carbon-to-carbon unsaturated bonds

Abstract

<PICT:0738171/IV (b)/1> A continuous process for preparing propylene chlorhydrin from water, chlorine and propylene is characterized by operation at a temperature below 60 DEG C., with a volume of propylene-containing gas of which a maximum of 50 per cent is consumed in the reaction, in an apparatus comprising two distinct superposed reaction zones; the first said zone for dissolving the chlorine in the propylene chlorhydrin aqueous solution, the second said zone for reacting the chlorine-containing solution with the propylene and piping connecting the top of the second zone with the bottom of the first zone, said apparatus affording gravitational recirculation of the chlorhydrin solution between both reaction zones in consequence of the buoyancy of both gases introduced and of the different densities of the gaseous dispersion in the reaction zones on the one hand and of the liquid in the recirculation piping on the other hand whereby the concentrations of free dissolved chlorine and of chlorine transformed into hypochlorous acid taken together and expressed as chlorine are maintained at a value lower than 0.5 gram per litre. An excess of propylene compared with the introduced chlorine may be employed or a diluent may be used, e.g. a paraffin hydrocarbon such as ethane, propane or the butanes usually accompanying propylene in the fraction of liquefied petroleum gases rich in this olefine or any other gas inert under the reaction conditions such as methane, hydrogen or nitrogen. The apparatus in the drawing is filled to the upper level of tube 10 with an aqueous solution containing propylene chlorhydrin whilst a stream of chlorine gas is introduced into column 1 through porous plate 2, with the formation of hypochlorous acid which reacts in column 3 with diluted propylene introduced through porous plate 4. The solution of propylene chlorhydrin is partially withdrawn through tubing 10 and partially recirculated through tubing 5, water being introduced at 6 at a rate corresponding to the rate of withdrawal through 10. The solution is recirculated through tubing 7 and adjustment device 8 to column 1. The residual gases are recovered at 9. In the examples: propylene chlorhydrin is produced using the above apparatus and as propylene containing starting material a mixture of propylene, propane and hydrocarbons having four carbon atoms (1); and a mixture of propylene, ethylene, ethane, propane and butanes. Specification 450,372 is referred to.
GB2712752A 1952-10-28 1952-10-28 Process for the preparation of propylene chlorhydrin Expired GB738171A (en)

Priority Applications (1)

Application Number Priority Date Filing Date Title
GB2712752A GB738171A (en) 1952-10-28 1952-10-28 Process for the preparation of propylene chlorhydrin

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
GB2712752A GB738171A (en) 1952-10-28 1952-10-28 Process for the preparation of propylene chlorhydrin

Publications (1)

Publication Number Publication Date
GB738171A true GB738171A (en) 1955-10-12

Family

ID=10254658

Family Applications (1)

Application Number Title Priority Date Filing Date
GB2712752A Expired GB738171A (en) 1952-10-28 1952-10-28 Process for the preparation of propylene chlorhydrin

Country Status (1)

Country Link
GB (1) GB738171A (en)

Cited By (3)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
DE1063140B (en) * 1957-12-06 1959-08-13 Basf Ag Process for the continuous production of propylene chlorohydrin
US2902519A (en) * 1957-01-09 1959-09-01 Allied Chem Manufacture of chlorohydrins
DE1211140B (en) * 1962-04-02 1966-02-24 Shell Int Research Process for the production of chlorohydrins

Cited By (3)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US2902519A (en) * 1957-01-09 1959-09-01 Allied Chem Manufacture of chlorohydrins
DE1063140B (en) * 1957-12-06 1959-08-13 Basf Ag Process for the continuous production of propylene chlorohydrin
DE1211140B (en) * 1962-04-02 1966-02-24 Shell Int Research Process for the production of chlorohydrins

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