FR2366242A1 - Procede de preparation de b-isopropyl-naphtalene - Google Patents
Procede de preparation de b-isopropyl-naphtaleneInfo
- Publication number
- FR2366242A1 FR2366242A1 FR7729656A FR7729656A FR2366242A1 FR 2366242 A1 FR2366242 A1 FR 2366242A1 FR 7729656 A FR7729656 A FR 7729656A FR 7729656 A FR7729656 A FR 7729656A FR 2366242 A1 FR2366242 A1 FR 2366242A1
- Authority
- FR
- France
- Prior art keywords
- naphthalene
- isopropyl
- beta
- propylene
- bars
- 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.)
- Granted
Links
Classifications
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
- C07C15/00—Cyclic hydrocarbons containing only six-membered aromatic rings as cyclic parts
- C07C15/20—Polycyclic condensed hydrocarbons
- C07C15/24—Polycyclic condensed hydrocarbons containing two rings
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
- C07C2/00—Preparation of hydrocarbons from hydrocarbons containing a smaller number of carbon atoms
- C07C2/54—Preparation of hydrocarbons from hydrocarbons containing a smaller number of carbon atoms by addition of unsaturated hydrocarbons to saturated hydrocarbons or to hydrocarbons containing a six-membered aromatic ring with no unsaturation outside the aromatic ring
- C07C2/64—Addition to a carbon atom of a six-membered aromatic ring
- C07C2/66—Catalytic processes
- C07C2/70—Catalytic processes with acids
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
- C07C5/00—Preparation of hydrocarbons from hydrocarbons containing the same number of carbon atoms
- C07C5/22—Preparation of hydrocarbons from hydrocarbons containing the same number of carbon atoms by isomerisation
- C07C5/27—Rearrangement of carbon atoms in the hydrocarbon skeleton
- C07C5/2729—Changing the branching point of an open chain or the point of substitution on a ring
- C07C5/2732—Catalytic processes
- C07C5/274—Catalytic processes with inorganic acids; with salts or anhydrides of acids
- C07C5/2745—Acids of phosphorus; Salts thereof; Phosphorus acids
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
- C07C2521/00—Catalysts comprising the elements, oxides or hydroxides of magnesium, boron, aluminium, carbon, silicon, titanium, zirconium or hafnium
- C07C2521/06—Silicon, titanium, zirconium or hafnium; Oxides or hydroxides thereof
- C07C2521/08—Silica
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
- C07C2527/00—Catalysts comprising the elements or compounds of halogens, sulfur, selenium, tellurium, phosphorus or nitrogen; Catalysts comprising carbon compounds
- C07C2527/14—Phosphorus; Compounds thereof
- C07C2527/16—Phosphorus; Compounds thereof containing oxygen
- C07C2527/167—Phosphates or other compounds comprising the anion (PnO3n+1)(n+2)-
- C07C2527/173—Phosphoric acid or other acids with the formula Hn+2PnO3n+1
Landscapes
- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Chemical Kinetics & Catalysis (AREA)
- Inorganic Chemistry (AREA)
- Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)
- Low-Molecular Organic Synthesis Reactions Using Catalysts (AREA)
Abstract
La présente invention est relative à un procédé de préparation de beta -isopropyl-naphtalène par conversion de naphtalène avec du propylène, en présence d'un catalyseur à base d'acide phosphorique déposé sur SiO2 (1**re étape), puis par isomérisation de l' alpha -iscpropyl-naphtalène et du beta -isopropyl-naphtalène (2**e étape), caractérisé en ce que, dans la première étape, on fait réagir progressivement sur du naphtalène liquéfié, à une température de 150 à 280 degrés et sous une pression de 5 à 30 bars, du propylène dans un rapport molaire de 1/5 à 1/20 mole de propylène par mole de naphtalène de départ, jusqu'à ce que 45 à 65 % du naphtalène soient isopropylés et on chauffe ensuite le mélange réactionnel jusqu'à 180 à 280 degrés C, sans séparation préalable du naphtalène non converti, en opérant également en présence d'un catalyseur à base d'acide phosphorique et sous une pression de gaz inerte de 5 à 30 bars, jusqu'à ce qu'il ne se forme pratiquement. plus dans le mélange d'isomères de beta -isopropyl-naphtalène et on isole le beta -isopropyl-naphtalène du mélange réactionnel.
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
DE2644624A DE2644624C2 (de) | 1976-10-02 | 1976-10-02 | Verfahren zur Herstellung von β-Isopropyl-naphthalin |
Publications (2)
Publication Number | Publication Date |
---|---|
FR2366242A1 true FR2366242A1 (fr) | 1978-04-28 |
FR2366242B1 FR2366242B1 (fr) | 1980-10-03 |
Family
ID=5989557
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
FR7729656A Granted FR2366242A1 (fr) | 1976-10-02 | 1977-10-03 | Procede de preparation de b-isopropyl-naphtalene |
Country Status (5)
Country | Link |
---|---|
US (1) | US4440957A (fr) |
JP (1) | JPS5350146A (fr) |
DE (1) | DE2644624C2 (fr) |
FR (1) | FR2366242A1 (fr) |
GB (1) | GB1538367A (fr) |
Cited By (1)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
FR2498177A1 (fr) * | 1981-01-16 | 1982-07-23 | Ugine Kuhlmann | Preparation regioselective du b-isopropylnaphtalene sur des catalyseurs superacides solides ou supportes a base d'acides perfluorosulfoniques |
Families Citing this family (4)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
GB8423636D0 (en) * | 1984-09-19 | 1984-11-14 | Fisons Plc | Analytical solutions |
JPH01197448A (ja) * | 1988-02-01 | 1989-08-09 | Chiyoda Corp | ナフタレンからのジイソプロピルナフタレンの製造方法 |
US5839313A (en) * | 1998-02-18 | 1998-11-24 | Danieli United, A Division Of Danieli Corporation | Rolling mill with intermediate crossed rolls background |
CN114031116B (zh) * | 2021-12-24 | 2022-10-14 | 中南大学 | β型四钼酸铵的制备方法 |
Family Cites Families (5)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US3458587A (en) * | 1967-11-14 | 1969-07-29 | Sun Oil Co | Preparation of beta-isopropylnaphthalene |
US3504046A (en) * | 1968-04-26 | 1970-03-31 | American Cyanamid Co | Alkylation of naphthalene with propylene in the presence of phosphoric acid catalyst |
US3504045A (en) * | 1969-06-03 | 1970-03-31 | American Cyanamid Co | Isomerization of alpha isopropyl naphthalene to beta isopropyl naphthalene |
JPS5622087B2 (fr) * | 1972-09-08 | 1981-05-23 | ||
US3813451A (en) * | 1973-01-16 | 1974-05-28 | Monsanto Co | Process for alkylation of aromatic compounds |
-
1976
- 1976-10-02 DE DE2644624A patent/DE2644624C2/de not_active Expired
-
1977
- 1977-09-30 JP JP11695977A patent/JPS5350146A/ja active Granted
- 1977-10-03 GB GB41048/77A patent/GB1538367A/en not_active Expired
- 1977-10-03 FR FR7729656A patent/FR2366242A1/fr active Granted
-
1981
- 1981-08-03 US US06/289,525 patent/US4440957A/en not_active Expired - Fee Related
Cited By (1)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
FR2498177A1 (fr) * | 1981-01-16 | 1982-07-23 | Ugine Kuhlmann | Preparation regioselective du b-isopropylnaphtalene sur des catalyseurs superacides solides ou supportes a base d'acides perfluorosulfoniques |
Also Published As
Publication number | Publication date |
---|---|
GB1538367A (en) | 1979-01-17 |
DE2644624C2 (de) | 1987-02-19 |
JPS5350146A (en) | 1978-05-08 |
JPS5761253B2 (fr) | 1982-12-23 |
FR2366242B1 (fr) | 1980-10-03 |
US4440957A (en) | 1984-04-03 |
DE2644624A1 (de) | 1978-04-06 |
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Legal Events
Date | Code | Title | Description |
---|---|---|---|
ST | Notification of lapse |