BE421095A - - Google Patents
Info
- Publication number
 - BE421095A BE421095A BE421095DA BE421095A BE 421095 A BE421095 A BE 421095A BE 421095D A BE421095D A BE 421095DA BE 421095 A BE421095 A BE 421095A
 - Authority
 - BE
 - Belgium
 - Prior art keywords
 - anhydride
 - aluminum
 - carboxylic
 - acid
 - carboxylic acid
 - Prior art date
 
Links
- XAGFODPZIPBFFR-UHFFFAOYSA-N aluminium Chemical compound [Al] XAGFODPZIPBFFR-UHFFFAOYSA-N 0.000 claims description 18
 - AZDRQVAHHNSJOQ-UHFFFAOYSA-N alumane Chemical class [AlH3] AZDRQVAHHNSJOQ-UHFFFAOYSA-N 0.000 claims description 12
 - 150000001732 carboxylic acid derivatives Chemical class 0.000 claims description 11
 - 238000000034 method Methods 0.000 claims description 11
 - 150000008064 anhydrides Chemical class 0.000 claims description 9
 - 230000007935 neutral effect Effects 0.000 claims description 9
 - 150000001244 carboxylic acid anhydrides Chemical class 0.000 claims description 7
 - 150000001735 carboxylic acids Chemical class 0.000 claims description 5
 - 238000002360 preparation method Methods 0.000 claims description 4
 - 238000010438 heat treatment Methods 0.000 claims description 3
 - 125000004432 carbon atom Chemical group C* 0.000 claims description 2
 - 229910052782 aluminium Inorganic materials 0.000 description 15
 - WFDIJRYMOXRFFG-UHFFFAOYSA-N Acetic anhydride Chemical compound CC(=O)OC(C)=O WFDIJRYMOXRFFG-UHFFFAOYSA-N 0.000 description 12
 - 239000002253 acid Substances 0.000 description 10
 - 150000003839 salts Chemical class 0.000 description 7
 - QTBSBXVTEAMEQO-UHFFFAOYSA-N Acetic acid Chemical compound CC(O)=O QTBSBXVTEAMEQO-UHFFFAOYSA-N 0.000 description 6
 - 239000000203 mixture Substances 0.000 description 5
 - FERIUCNNQQJTOY-UHFFFAOYSA-N Butyric acid Chemical compound CCCC(O)=O FERIUCNNQQJTOY-UHFFFAOYSA-N 0.000 description 4
 - 238000009835 boiling Methods 0.000 description 4
 - XBDQKXXYIPTUBI-UHFFFAOYSA-N dimethylselenoniopropionate Natural products CCC(O)=O XBDQKXXYIPTUBI-UHFFFAOYSA-N 0.000 description 4
 - HDYRYUINDGQKMC-UHFFFAOYSA-M acetyloxyaluminum;dihydrate Chemical compound O.O.CC(=O)O[Al] HDYRYUINDGQKMC-UHFFFAOYSA-M 0.000 description 3
 - 229940009827 aluminum acetate Drugs 0.000 description 3
 - MNWFXJYAOYHMED-UHFFFAOYSA-N heptanoic acid Chemical compound CCCCCCC(O)=O MNWFXJYAOYHMED-UHFFFAOYSA-N 0.000 description 3
 - 230000003213 activating effect Effects 0.000 description 2
 - 150000001447 alkali salts Chemical class 0.000 description 2
 - WPCPXPTZTOMGRF-UHFFFAOYSA-K di(butanoyloxy)alumanyl butanoate Chemical compound [Al+3].CCCC([O-])=O.CCCC([O-])=O.CCCC([O-])=O WPCPXPTZTOMGRF-UHFFFAOYSA-K 0.000 description 2
 - 235000019260 propionic acid Nutrition 0.000 description 2
 - WYVAMUWZEOHJOQ-UHFFFAOYSA-N propionic anhydride Chemical compound CCC(=O)OC(=O)CC WYVAMUWZEOHJOQ-UHFFFAOYSA-N 0.000 description 2
 - IUVKMZGDUIUOCP-BTNSXGMBSA-N quinbolone Chemical compound O([C@H]1CC[C@H]2[C@H]3[C@@H]([C@]4(C=CC(=O)C=C4CC3)C)CC[C@@]21C)C1=CCCC1 IUVKMZGDUIUOCP-BTNSXGMBSA-N 0.000 description 2
 - 238000007514 turning Methods 0.000 description 2
 - 239000002699 waste material Substances 0.000 description 2
 - XBDQKXXYIPTUBI-UHFFFAOYSA-M Propionate Chemical compound CCC([O-])=O XBDQKXXYIPTUBI-UHFFFAOYSA-M 0.000 description 1
 - 150000007513 acids Chemical class 0.000 description 1
 - MPPKCHCSXZJSIC-UHFFFAOYSA-K aluminum;heptanoate Chemical compound [Al+3].CCCCCCC([O-])=O.CCCCCCC([O-])=O.CCCCCCC([O-])=O MPPKCHCSXZJSIC-UHFFFAOYSA-K 0.000 description 1
 - DMGNPLVEZUUCBT-UHFFFAOYSA-K aluminum;propanoate Chemical compound [Al+3].CCC([O-])=O.CCC([O-])=O.CCC([O-])=O DMGNPLVEZUUCBT-UHFFFAOYSA-K 0.000 description 1
 - YHASWHZGWUONAO-UHFFFAOYSA-N butanoyl butanoate Chemical compound CCCC(=O)OC(=O)CCC YHASWHZGWUONAO-UHFFFAOYSA-N 0.000 description 1
 - 239000003795 chemical substances by application Substances 0.000 description 1
 - 150000001991 dicarboxylic acids Chemical class 0.000 description 1
 - 230000000694 effects Effects 0.000 description 1
 - 238000001914 filtration Methods 0.000 description 1
 - MNWFXJYAOYHMED-UHFFFAOYSA-M heptanoate Chemical compound CCCCCCC([O-])=O MNWFXJYAOYHMED-UHFFFAOYSA-M 0.000 description 1
 - DAPZDAPTZFJZTO-UHFFFAOYSA-N heptanoyl heptanoate Chemical compound CCCCCCC(=O)OC(=O)CCCCCC DAPZDAPTZFJZTO-UHFFFAOYSA-N 0.000 description 1
 - 238000004519 manufacturing process Methods 0.000 description 1
 - 239000000843 powder Substances 0.000 description 1
 - 238000000926 separation method Methods 0.000 description 1
 - 238000003860 storage Methods 0.000 description 1
 
Classifications
- 
        
- C—CHEMISTRY; METALLURGY
 - C07—ORGANIC CHEMISTRY
 - C07F—ACYCLIC, CARBOCYCLIC OR HETEROCYCLIC COMPOUNDS CONTAINING ELEMENTS OTHER THAN CARBON, HYDROGEN, HALOGEN, OXYGEN, NITROGEN, SULFUR, SELENIUM OR TELLURIUM
 - C07F5/00—Compounds containing elements of Groups 3 or 13 of the Periodic Table
 - C07F5/06—Aluminium compounds
 - C07F5/069—Aluminium compounds without C-aluminium linkages
 
 
Landscapes
- Chemical & Material Sciences (AREA)
 - Organic Chemistry (AREA)
 - Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)
 
Publications (1)
| Publication Number | Publication Date | 
|---|---|
| BE421095A true BE421095A (h) | 
Family
ID=83027
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date | 
|---|---|---|---|
| BE421095D BE421095A (h) | 
Country Status (1)
| Country | Link | 
|---|---|
| BE (1) | BE421095A (h) | 
- 
        0
        
- BE BE421095D patent/BE421095A/fr unknown
 
 
Similar Documents
| Publication | Publication Date | Title | 
|---|---|---|
| EP1351917B1 (fr) | Compositions stabilisees d'acide o-iodoxybenzoique et leur procede de preparation | |
| JP2001072642A (ja) | ポリマー又はポリアミドの合成に適したジカルボン酸の製造方法 | |
| BE421095A (h) | ||
| EP0390905B1 (fr) | Composes amidofluores, leur obtention et leur utilisation | |
| CA1265153A (fr) | Synthese des tetrahydro-1,1,2,2 perfluoroalcanols et de leurs esters | |
| EP2917176A1 (fr) | Extraction selective d'un acide omega-fonctionnalise apres coupure oxydante d'un acide gras insature et derives | |
| EP0072293A2 (fr) | Procédé de préparation de l'acide ursodésoxycholique à partir de l'acide 3 alpha, 7 beta, 12 alpha-trihydroxycholanique et produits intermédiaires utilisés | |
| BE877108A (fr) | Procede d'obtention de sels de plomb en partant de sulfate de plomb | |
| BE448884A (h) | ||
| BE455144A (h) | ||
| BE431257A (h) | ||
| JPS597132A (ja) | 3−メチル−3−ヒドロキシグルタル酸の製造法及びその製造用中間体化合物 | |
| BE505572A (h) | ||
| BE521054A (h) | ||
| BE574797A (h) | ||
| BE516402A (h) | ||
| BE500212A (h) | ||
| BE560450A (h) | ||
| BE417716A (h) | ||
| BE454056A (h) | ||
| FR2573754A1 (fr) | Procede de preparation d'acides a-hydroxyphenylalcanoiques et composes obtenus par ce procede | |
| BE555380A (h) | ||
| BE455250A (h) | ||
| BE450950A (h) | ||
| BE521780A (h) |