GB299373A - - Google Patents

Info

Publication number
GB299373A
GB299373A GB30810/28A GB3081028A GB299373A GB 299373 A GB299373 A GB 299373A GB 30810/28 A GB30810/28 A GB 30810/28A GB 3081028 A GB3081028 A GB 3081028A GB 299373 A GB299373 A GB 299373A
Authority
GB
United Kingdom
Prior art keywords
glycerine
dihydroxypropane
water
atmospheres
cellulose
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
GB30810/28A
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.)
IG Farbenindustrie AG
Original Assignee
IG Farbenindustrie 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 IG Farbenindustrie AG filed Critical IG Farbenindustrie AG
Publication of GB299373A publication Critical patent/GB299373A/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
    • 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
    • C07C29/09Preparation of compounds having hydroxy or O-metal groups bound to a carbon atom not belonging to a six-membered aromatic ring by hydrolysis
    • C07C29/10Preparation of compounds having hydroxy or O-metal groups bound to a carbon atom not belonging to a six-membered aromatic ring by hydrolysis of ethers, including cyclic ethers, e.g. oxiranes

Landscapes

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

Abstract

299,373. I. G. Farbenindustrie Akt.- Ges. Oct. 24, 1927, [Convention date]. Alcohols; ethers.-Polylydroxy compounds are hydrogenated by treatment in solution or suspension in water with hydrogen in presence of a hydrogenating catalyst under raised pressure and at, a temperature not exceeding 300‹ C. The process is particularly applicable to sugars, starch, cellulose, glycerine, hexites, glucosans and polyhydroxy acids such as gluconic acid; glycerine and its further restriction product, 1 : 2-dihydroxypropane, comprise the main products. Pressures of 70-100 atmospheres are usually employed, and the temperature is preferably above 200‹ C. The hydrogenating catalysts used are those of the iron and platinum groups, alone or in combination. Examples are given of the production of a mixture of dihydroxypropane and glycerine by treatment of sorbite, dextrose, cane sugar, starch and cellulose using nickel as catalyst. The hydrogenation of glucose to produce first the hexite and then glycerine is mentioned. Specification 309,200 is referred to. The Specification as open to inspection under Sect. 91 (3) (a) is not confined to the presence of water or to a temperature limit of 300‹ C. It refers to the use of pressures of 10-60 atmospheres, 200 atmospheres and even 1,000 atmospheres. The following catalysts are also specified :-copper, silver, gold, tungstic acid, or mixtures thereof, mounted if desired on a carrier such as pumice, silicic acid and asbestos; also nickel oxide, a mixture of nickel, cobalt and copper, or a mixture of cobalt and copper. It states that the reaction may be effected in the presence of a solvent and that in some cases another gas such as carbon dioxide may be present. It describes the treatment of straw, peat and sawdust to produce dihydroxypropane and glycerine; in the case of sawdust, there may also be obtained mannite and isopropyl alcohol. It includes additional examples of the production of dihydroxypropane from glycerine in the absence of water or other solvent, dimethoxy- (or diethoxy) -trihydroxyhexane from dimethyl- (or diethyl)- cellulose in presence of water, and dihydroxypropane, glycerine and isosorbide from cellulose in presence of water. This subject-matter does not appear in the Specification as accepted.
GB30810/28A 1927-10-24 1928-10-24 Expired GB299373A (en)

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
DE299373T 1927-10-24

Publications (1)

Publication Number Publication Date
GB299373A true GB299373A (en) 1930-02-24

Family

ID=31894219

Family Applications (1)

Application Number Title Priority Date Filing Date
GB30810/28A Expired GB299373A (en) 1927-10-24 1928-10-24

Country Status (1)

Country Link
GB (1) GB299373A (en)

Cited By (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US5306847A (en) * 1991-11-26 1994-04-26 Basf Aktiengesellschaft Manufacture of 1,2-propylene glycol

Cited By (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US5306847A (en) * 1991-11-26 1994-04-26 Basf Aktiengesellschaft Manufacture of 1,2-propylene glycol

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