GB803060A - Process for the production of lactic acid and derivatives - Google Patents

Process for the production of lactic acid and derivatives

Info

Publication number
GB803060A
GB803060A GB36857/56A GB3685756A GB803060A GB 803060 A GB803060 A GB 803060A GB 36857/56 A GB36857/56 A GB 36857/56A GB 3685756 A GB3685756 A GB 3685756A GB 803060 A GB803060 A GB 803060A
Authority
GB
United Kingdom
Prior art keywords
lactic acid
nitric acid
mol
acid
propylene
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
GB36857/56A
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.)
Escambia Chemical Corp
Original Assignee
Escambia Chemical Corp
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 Escambia Chemical Corp filed Critical Escambia Chemical Corp
Publication of GB803060A publication Critical patent/GB803060A/en
Expired legal-status Critical Current

Links

Classifications

    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07CACYCLIC OR CARBOCYCLIC COMPOUNDS
    • C07C51/00Preparation of carboxylic acids or their salts, halides or anhydrides
    • C07C51/16Preparation of carboxylic acids or their salts, halides or anhydrides by oxidation
    • C07C51/27Preparation of carboxylic acids or their salts, halides or anhydrides by oxidation with oxides of nitrogen or nitrogen-containing mineral acids
    • C07C51/275Preparation of carboxylic acids or their salts, halides or anhydrides by oxidation with oxides of nitrogen or nitrogen-containing mineral acids of hydrocarbyl groups
    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07CACYCLIC OR CARBOCYCLIC COMPOUNDS
    • C07C51/00Preparation of carboxylic acids or their salts, halides or anhydrides
    • C07C51/347Preparation of carboxylic acids or their salts, halides or anhydrides by reactions not involving formation of carboxyl groups
    • C07C51/377Preparation of carboxylic acids or their salts, halides or anhydrides by reactions not involving formation of carboxyl groups by splitting-off hydrogen or functional groups; by hydrogenolysis of functional groups

Landscapes

  • Chemical & Material Sciences (AREA)
  • Organic Chemistry (AREA)
  • Engineering & Computer Science (AREA)
  • Oil, Petroleum & Natural Gas (AREA)
  • Chemical Kinetics & Catalysis (AREA)
  • Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)

Abstract

Lactic acid is prepared by contacting propylene at a temperature below about 40 DEG C. with an oxidizing medium containing at least one mol. of dinitrogen tetroxide (nitrogen dioxide), dinitrogen trioxide or a mixture thereof for each mol. of propylene, and reacting the resulting reaction products with at least one mol. of nitric acid for each mol. of propylene. The nitric acid may be present in the oxidizing medium or may subsequently be added to the reaction products or, preferably, the reaction products added to it. Nitric acid with an HNO3 concentration of 25-100 per cent by weight is suitable. It may be formed in situ, e.g. by reaction of added water with N2O4. When the oxidizing medium contains both nitric acid and the oxidizing agent, reaction temperatures below about 10 DEG C. are desirable. When two steps are used, the first is preferably effected below about 10 DEG C., but the step employing nitric acid may be effected at temperatures as high as 100 DEG C. An hydrolysis step may be necessary to obtain maximum yield of lactic acid. The lactic acid may be dehydrated to acrylic acid and/or esterified, e.g. with alkanols, or esterified then dehydrated. Dehydration may be with P2O5 or by the methods described in Specification 409,733, [Group IV]. An example is given in which the lactic acid is isolated as the calcium salt. Reference has been directed by the Comptroller to Specification 785,152.
GB36857/56A 1955-12-29 1956-12-03 Process for the production of lactic acid and derivatives Expired GB803060A (en)

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
US556067A US2847464A (en) 1955-12-29 1955-12-29 Preparation of lactic acid

Publications (1)

Publication Number Publication Date
GB803060A true GB803060A (en) 1958-10-15

Family

ID=24219768

Family Applications (1)

Application Number Title Priority Date Filing Date
GB36857/56A Expired GB803060A (en) 1955-12-29 1956-12-03 Process for the production of lactic acid and derivatives

Country Status (3)

Country Link
US (1) US2847464A (en)
DE (1) DE1114177B (en)
GB (1) GB803060A (en)

Families Citing this family (4)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US3081345A (en) * 1960-08-23 1963-03-12 Allied Chem Production of oxalic acid
NL269224A (en) * 1961-09-14
US3456005A (en) * 1966-05-06 1969-07-15 Wyandotte Chemicals Corp Preparation of trichlorolactic acid
US4022823A (en) * 1974-07-29 1977-05-10 Chevron Research Company Citric acid and citramalic acid preparation

Family Cites Families (5)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US2511915A (en) * 1950-06-20 Production of chloronitro
DE742053C (en) * 1939-04-04 1943-11-22 Dr Paul Busse Process for the production of oxalic acid
NL62760C (en) * 1943-03-27
US2402315A (en) * 1944-01-04 1946-06-18 Solvay Process Co Preparation of nitrogen tetroxide addition products
US2525353A (en) * 1946-12-18 1950-10-10 Phillips Petroleum Co Process for the production of esters

Also Published As

Publication number Publication date
DE1114177B (en) 1961-09-28
US2847464A (en) 1958-08-12

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