GB702016A - Manufacture of a stable preparation of the molecular compound of 4-dimethylamino-1-phenyl-2:3-dimethyl-5-pyrazolone and butyl-chloral hydrate - Google Patents

Manufacture of a stable preparation of the molecular compound of 4-dimethylamino-1-phenyl-2:3-dimethyl-5-pyrazolone and butyl-chloral hydrate

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Publication number
GB702016A
GB702016A GB27839/51A GB2783951A GB702016A GB 702016 A GB702016 A GB 702016A GB 27839/51 A GB27839/51 A GB 27839/51A GB 2783951 A GB2783951 A GB 2783951A GB 702016 A GB702016 A GB 702016A
Authority
GB
United Kingdom
Prior art keywords
molecular compound
pyrazolone
dimethylamino
dimethyl
phenyl
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
GB27839/51A
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.)
Hoechst AG
Original Assignee
Hoechst AG
Farbwerke Hoechst AG
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 Hoechst AG, Farbwerke Hoechst AG filed Critical Hoechst AG
Publication of GB702016A publication Critical patent/GB702016A/en
Expired legal-status Critical Current

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Abstract

A stable preparation of the molecular compound of 4-dimethylamino-1-phenyl-2.3-dimethyl-5-pyrazolone and butyl-chloral hydrate is prepared by adding trisodium phosphate or hexamethylene tetramine as a stabilizing agent to the molecular compound during or after its manufacture from the components. The stabilized compound may be prepared by reacting butyl-chloral hydrate at a temperature of 30-35 DEG C. with 4-dimethylamino-1-phenyl-2 : 3-dimethyl-5-pyrazolone in the presence of a solvent and with the addition of 1-2 per cent. of the stabilizing agent. If desired, the stabilizing agent may be added to the finished molecular compound. Preferably the butyl-chloral hydrate contains less than 0.1 per cent. of free hydrochloric acid. In the examples the molecular compound of 4-dimethylamino-1-phenyl-2 : 3-dimethyl-5-pyrazolone and butylchloral hydrate is stabilized by the addition of hexamethylene tetramine (a) during the preparation of the compound and (b) after separating the molecular compound. Specification 15782/03 , [Class 2], is referred to.
GB27839/51A 1950-11-27 1951-11-27 Manufacture of a stable preparation of the molecular compound of 4-dimethylamino-1-phenyl-2:3-dimethyl-5-pyrazolone and butyl-chloral hydrate Expired GB702016A (en)

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
DE702016X 1950-11-27

Publications (1)

Publication Number Publication Date
GB702016A true GB702016A (en) 1954-01-06

Family

ID=6611981

Family Applications (1)

Application Number Title Priority Date Filing Date
GB27839/51A Expired GB702016A (en) 1950-11-27 1951-11-27 Manufacture of a stable preparation of the molecular compound of 4-dimethylamino-1-phenyl-2:3-dimethyl-5-pyrazolone and butyl-chloral hydrate

Country Status (1)

Country Link
GB (1) GB702016A (en)

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