GB682280A - Purification of ortho-methoxyphenylacetone - Google Patents

Purification of ortho-methoxyphenylacetone

Info

Publication number
GB682280A
GB682280A GB17600/50A GB1760050A GB682280A GB 682280 A GB682280 A GB 682280A GB 17600/50 A GB17600/50 A GB 17600/50A GB 1760050 A GB1760050 A GB 1760050A GB 682280 A GB682280 A GB 682280A
Authority
GB
United Kingdom
Prior art keywords
methoxyphenylacetone
bisulphite
solution
methoxybenzaldehyde
crude
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
GB17600/50A
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.)
Pharmacia and Upjohn Co
Original Assignee
Upjohn Co
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 Upjohn Co filed Critical Upjohn Co
Publication of GB682280A publication Critical patent/GB682280A/en
Expired legal-status Critical Current

Links

Classifications

    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07CACYCLIC OR CARBOCYCLIC COMPOUNDS
    • C07C45/00Preparation of compounds having >C = O groups bound only to carbon or hydrogen atoms; Preparation of chelates of such compounds
    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07CACYCLIC OR CARBOCYCLIC COMPOUNDS
    • C07C45/00Preparation of compounds having >C = O groups bound only to carbon or hydrogen atoms; Preparation of chelates of such compounds
    • C07C45/78Separation; Purification; Stabilisation; Use of additives
    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07CACYCLIC OR CARBOCYCLIC COMPOUNDS
    • C07C45/00Preparation of compounds having >C = O groups bound only to carbon or hydrogen atoms; Preparation of chelates of such compounds
    • C07C45/78Separation; Purification; Stabilisation; Use of additives
    • C07C45/80Separation; Purification; Stabilisation; Use of additives by liquid-liquid treatment
    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07CACYCLIC OR CARBOCYCLIC COMPOUNDS
    • C07C45/00Preparation of compounds having >C = O groups bound only to carbon or hydrogen atoms; Preparation of chelates of such compounds
    • C07C45/78Separation; Purification; Stabilisation; Use of additives
    • C07C45/85Separation; Purification; Stabilisation; Use of additives by treatment giving rise to a chemical modification

Landscapes

  • Chemical & Material Sciences (AREA)
  • Organic Chemistry (AREA)
  • Chemical Kinetics & Catalysis (AREA)
  • General Chemical & Material Sciences (AREA)
  • Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)
  • Low-Molecular Organic Synthesis Reactions Using Catalysts (AREA)

Abstract

In a method for the purification of o-methoxyphenylacetone containing as impurities one or more aldehydes and/or other ketones and/or one or more other organic compounds which form more readily than o-methoxyphenylacetone an addition complex with a bisulphite, crude o-methoxyphenylacetone is brought into contact with an alkali metal bisulphite, and the o-methoxyphenylacetone is separated in purified form from the complex formed between the bisulphite and the impurities present. The bisulphite may be in the form of finely-divided solid, but is preferably used in aqueous solution. The crude o-methoxy phenylacetone may be dissolved in a water-immiscible organic solvent, e.g. benzene, toluene, chloroform dichlorethane, ether, petroleum ether or ethyl acetate. Examples describe the separation of purified o-methoxyphenylacetone from a mixture of (1) a toluene solution of crude o-methoxyphenylacetone obtained by Experiment 2 of Specification 671,240, and aqueous sodium bisulphite solution; (2) the separated product of (1) and further bisulphite solution; (3) 85.5 per cent o-methoxyphenylacetone and 14.5 per cent o-methoxybenzaldehyde with solid sodium bisulphite; (4) as in (3) but with aqueous sodium bisulphite. The bisulphite addition compound is treated with concentrated hydrochloric acid and the liberated o-methoxybenzaldehyde is recovered; (5) a benzene solution of o-methoxyphenylacetone and o-methoxybenzaldehyde with aqueous sodium bisulphite.
GB17600/50A 1949-08-08 1950-07-13 Purification of ortho-methoxyphenylacetone Expired GB682280A (en)

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
US682280XA 1949-08-08 1949-08-08

Publications (1)

Publication Number Publication Date
GB682280A true GB682280A (en) 1952-11-05

Family

ID=22081219

Family Applications (1)

Application Number Title Priority Date Filing Date
GB17600/50A Expired GB682280A (en) 1949-08-08 1950-07-13 Purification of ortho-methoxyphenylacetone

Country Status (2)

Country Link
DE (1) DE892442C (en)
GB (1) GB682280A (en)

Cited By (2)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US5221992A (en) * 1991-02-20 1993-06-22 Park Ki K Door viewer including inner tube encasing object lenses and ocular lens and including a rubberized flexible hood
CN114858944A (en) * 2022-05-31 2022-08-05 石家庄四药有限公司 Method for detecting p-methoxypropiophenone related substances

Cited By (3)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US5221992A (en) * 1991-02-20 1993-06-22 Park Ki K Door viewer including inner tube encasing object lenses and ocular lens and including a rubberized flexible hood
CN114858944A (en) * 2022-05-31 2022-08-05 石家庄四药有限公司 Method for detecting p-methoxypropiophenone related substances
CN114858944B (en) * 2022-05-31 2023-02-03 石家庄四药有限公司 Method for detecting p-methoxypropiophenone related substances

Also Published As

Publication number Publication date
DE892442C (en) 1953-10-08

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