GB710406A - Trichloroacetates of the chloroaryloxyalkanols - Google Patents

Trichloroacetates of the chloroaryloxyalkanols

Info

Publication number
GB710406A
GB710406A GB26782/52A GB2678252A GB710406A GB 710406 A GB710406 A GB 710406A GB 26782/52 A GB26782/52 A GB 26782/52A GB 2678252 A GB2678252 A GB 2678252A GB 710406 A GB710406 A GB 710406A
Authority
GB
United Kingdom
Prior art keywords
propanol
ethanol
dichlorophenoxy
chlorophenoxy
reacting
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
GB26782/52A
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.)
Dow Chemical Co
Original Assignee
Dow Chemical 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 Dow Chemical Co filed Critical Dow Chemical Co
Publication of GB710406A publication Critical patent/GB710406A/en
Expired legal-status Critical Current

Links

Classifications

    • C—CHEMISTRY; METALLURGY
    • C07—ORGANIC CHEMISTRY
    • C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
    • C07C69/00—Esters of carboxylic acids; Esters of carbonic or haloformic acids
    • C07C69/62—Halogen-containing esters
    • C07C69/63—Halogen-containing esters of saturated acids

Landscapes

  • Chemical & Material Sciences (AREA)
  • Organic Chemistry (AREA)
  • Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)

Abstract

The invention comprises compounds of the formula CCl3CO.O.CnH2n.O.R, wherein n is 2 or 3 and R is a chloroaryl radical. Such compounds are obtained by reacting a molecular proportion of trichloracetic acid with at least a molecular proportion of the appropriate chloraryloxyalkanol, preferably with the removal of water as formed. The products may be used in soil sterilization. In example (1) 2-(2,4-dichlorophenoxy) ethyl trichloracetate is prepared by reacting 2-(2,4-dichlorophenoxy) ethanol and trichloracetic acid. Similarly obtained are the trichloracetates of (2), 1-(2,4-dichlorophenoxy)-2 - propanol; (3) 2 - (4 - chloro - o - toloxy) ethanol; (4) 2-(2,4,5-trichlorophenoxy) ethanol. Also mentioned are the trichloroacetates of 2 - (4 - chlorophenoxyethanol, 1 - (2,4,5 - trichlorophenoxy - 2 - propanol, 1 - (4 - chloro - o - tolyloxy) - 2 - propanol and 1 - (2 - chlorophenoxy)-2-propanol. Chloroaryloxyalkanols are obtained by reacting ethylene oxide or propylene oxide with the appropriate phenol. Additional alkanols mentioned are 2-(2-chlorophenoxy) ethanol and 1-(4-chlorophenoxy)-2-propanol.
GB26782/52A 1951-11-23 1952-10-24 Trichloroacetates of the chloroaryloxyalkanols Expired GB710406A (en)

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
US710406XA 1951-11-23 1951-11-23

Publications (1)

Publication Number Publication Date
GB710406A true GB710406A (en) 1954-06-09

Family

ID=22098884

Family Applications (1)

Application Number Title Priority Date Filing Date
GB26782/52A Expired GB710406A (en) 1951-11-23 1952-10-24 Trichloroacetates of the chloroaryloxyalkanols

Country Status (1)

Country Link
GB (1) GB710406A (en)

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