GB757564A - Continuous production of pentaerythritol - Google Patents

Continuous production of pentaerythritol

Info

Publication number
GB757564A
GB757564A GB15015/54A GB1501554A GB757564A GB 757564 A GB757564 A GB 757564A GB 15015/54 A GB15015/54 A GB 15015/54A GB 1501554 A GB1501554 A GB 1501554A GB 757564 A GB757564 A GB 757564A
Authority
GB
United Kingdom
Prior art keywords
formaldehyde
pentaerythritol
per cent
reaction
acetaldehyde
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
GB15015/54A
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.)
Celanese Corp
Original Assignee
Celanese Corp
Celanese Corp of America
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 Celanese Corp, Celanese Corp of America filed Critical Celanese Corp
Publication of GB757564A publication Critical patent/GB757564A/en
Expired legal-status Critical Current

Links

Classifications

    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07CACYCLIC OR CARBOCYCLIC COMPOUNDS
    • C07C31/00Saturated compounds having hydroxy or O-metal groups bound to acyclic carbon atoms
    • C07C31/18Polyhydroxylic acyclic alcohols
    • C07C31/22Trihydroxylic alcohols, e.g. glycerol
    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07CACYCLIC OR CARBOCYCLIC COMPOUNDS
    • C07C31/00Saturated compounds having hydroxy or O-metal groups bound to acyclic carbon atoms
    • C07C31/18Polyhydroxylic acyclic alcohols
    • C07C31/20Dihydroxylic alcohols
    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07CACYCLIC OR CARBOCYCLIC COMPOUNDS
    • C07C41/00Preparation of ethers; Preparation of compounds having groups, groups or groups
    • C07C41/48Preparation of compounds having groups
    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07CACYCLIC OR CARBOCYCLIC COMPOUNDS
    • C07C41/00Preparation of ethers; Preparation of compounds having groups, groups or groups
    • C07C41/48Preparation of compounds having groups
    • C07C41/50Preparation of compounds having groups by reactions producing groups
    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07CACYCLIC OR CARBOCYCLIC COMPOUNDS
    • C07C41/00Preparation of ethers; Preparation of compounds having groups, groups or groups
    • C07C41/48Preparation of compounds having groups
    • C07C41/50Preparation of compounds having groups by reactions producing groups
    • C07C41/56Preparation of compounds having groups by reactions producing groups by condensation of aldehydes, paraformaldehyde, or ketones
    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07CACYCLIC OR CARBOCYCLIC COMPOUNDS
    • C07C43/00Ethers; Compounds having groups, groups or groups
    • C07C43/30Compounds having groups
    • 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
    • C07C45/61Preparation of compounds having >C = O groups bound only to carbon or hydrogen atoms; Preparation of chelates of such compounds by reactions not involving the formation of >C = O groups
    • C07C45/67Preparation of compounds having >C = O groups bound only to carbon or hydrogen atoms; Preparation of chelates of such compounds by reactions not involving the formation of >C = O groups by isomerisation; by change of size of the carbon skeleton
    • C07C45/68Preparation of compounds having >C = O groups bound only to carbon or hydrogen atoms; Preparation of chelates of such compounds by reactions not involving the formation of >C = O groups by isomerisation; by change of size of the carbon skeleton by increase in the number of carbon atoms
    • C07C45/72Preparation of compounds having >C = O groups bound only to carbon or hydrogen atoms; Preparation of chelates of such compounds by reactions not involving the formation of >C = O groups by isomerisation; by change of size of the carbon skeleton by increase in the number of carbon atoms by reaction of compounds containing >C = O groups with the same or other compounds containing >C = O groups
    • C07C45/75Reactions with formaldehyde

Landscapes

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

Abstract

Pentaerythritol is prepared by a continuous process of condensing acetaldehyde with formaldehyde comprising forming an aqueous stream containing acetaldehyde, a substantial excess of formaldehyde and an inorganic base, the inorganic base being introduced in a manner such that thorough mixing is effected in less than 2 minutes, passing the aqueous stream through a reaction zone in which it remains for a time sufficient for reaction to proceed to the desired extent, acidifying the effluent from the reaction zone, continuously distilling formaldehyde from the acidified effluent and recovering a pentaerythritol containing liquor. Suitable inorganic bases are for example, sodium hydroxide, calcium hydroxide or potassium hydroxide. A preferred starting mixture contains (by weight) 3 per cent of acetaldehyde, 20 per cent of formaldehyde and 77 per cent of water and it is desirable that the formaldehyde should contain less than 1 per cent of methanol based on the total weight of the mixture. The preferred reaction temperature is 130-140 DEG F. The alkaline mixture leaving the reactor should be acidified, for example, by addition of acetic acid, formic acid, sulphuric acid or hydrochloric acid, to prevent side reactions. The reaction liquor is then distilled to separate aqueous unreacted formaldehyde as distillate, leaving behind an aqueous solution of pentaerythritol and other non-volatile reaction products. Preferably some of the formaldehyde-containing distillate is recycled. After the distillation the pentaerythritol-containing liquor may be concentrated and cooled to crystallize out the pentaerythritol which may be further purified by recrystallization or otherwise.
GB15015/54A 1953-05-21 1954-05-21 Continuous production of pentaerythritol Expired GB757564A (en)

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
US757564XA 1953-05-21 1953-05-21

Publications (1)

Publication Number Publication Date
GB757564A true GB757564A (en) 1956-09-19

Family

ID=22127788

Family Applications (1)

Application Number Title Priority Date Filing Date
GB15015/54A Expired GB757564A (en) 1953-05-21 1954-05-21 Continuous production of pentaerythritol

Country Status (1)

Country Link
GB (1) GB757564A (en)

Cited By (3)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
DE1153739B (en) * 1958-12-15 1963-09-05 Meissner Fa Josef Process and device for the production of higher polyhydric alcohols
CN106349042A (en) * 2016-08-30 2017-01-25 安徽金禾实业股份有限公司 Method for producing energy-saving pentaerythritol deacetylation tower
CN110721554A (en) * 2019-11-19 2020-01-24 安徽金禾实业股份有限公司 Comprehensive utilization method for pentaerythritol production wastewater and formaldehyde acetaldehyde

Cited By (4)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
DE1153739B (en) * 1958-12-15 1963-09-05 Meissner Fa Josef Process and device for the production of higher polyhydric alcohols
CN106349042A (en) * 2016-08-30 2017-01-25 安徽金禾实业股份有限公司 Method for producing energy-saving pentaerythritol deacetylation tower
CN106349042B (en) * 2016-08-30 2018-11-06 安徽金禾实业股份有限公司 A kind of pentaerythrite dealdehyder tower energy-saving production method
CN110721554A (en) * 2019-11-19 2020-01-24 安徽金禾实业股份有限公司 Comprehensive utilization method for pentaerythritol production wastewater and formaldehyde acetaldehyde

Similar Documents

Publication Publication Date Title
Cope et al. Cyclic Polyolefins. XLII. 3, 3, 7, 7-Tetracarbethoxybicyclo [3.3. 0] oct-1 (5)-ene and 3, 3, 7, 7-Tetracarbethoxycycloöctane-1, 5-dione
US2401749A (en) Manufacture of pentaerythritol
US2140469A (en) Production of methacryl-containing compounds
US3564062A (en) Production of nitroalkanols
Boxer et al. C.—Investigations of the olefinic acids. Part V. The influence of bases on the condensation of aldehydes and malonic acid, and a note on the Knoevenagel reaction
GB757564A (en) Continuous production of pentaerythritol
US3187050A (en) Process for conditioning reducible cyclic organic compounds
US2121183A (en) Process for the manufacture of condensation products of dicarboxylic acid anhydrides
US2454047A (en) Conversion of alicyclic aldehydes
US4230869A (en) Process for preparing 5-(4-hydroxyphenyl)hydantoin
US2333696A (en) Chemical process
US2396292A (en) Acetylation of hydroxy nitriles
US1937477A (en) Process of preparing para-hydroxybenzoic acid
US2303842A (en) Process for producing unsaturated aliphatic compounds
GB742159A (en) Production of pentaerythritol
JPH05271143A (en) Production of cyclohexanone
US3153089A (en) Production of acetophenone-azine
US2878266A (en) Chloromethylation process
US2246049A (en) Process of preparing glyoxal
US2897239A (en) Process for the production of cumene hydro-peroxide
US2729670A (en) Manufacture of acrylonitrile
US3122584A (en) Production of ammonium formate
US2739157A (en) Racemization of alpha-hydroxy-beta,beta-dimethyl-gamma-butyrolactone
US2041593A (en) Process of hydrolyzing chlor alkyl phenols
US3017425A (en) Method for the preparation of monocyanoethylformamide