ES357649A1 - Un procedimiento para la producccion de una lactona insaturada. - Google Patents
Un procedimiento para la producccion de una lactona insaturada.Info
- Publication number
- ES357649A1 ES357649A1 ES357649A ES357649A ES357649A1 ES 357649 A1 ES357649 A1 ES 357649A1 ES 357649 A ES357649 A ES 357649A ES 357649 A ES357649 A ES 357649A ES 357649 A1 ES357649 A1 ES 357649A1
- Authority
- ES
- Spain
- Prior art keywords
- acid
- lactone
- production
- decalactone
- hydroxy
- 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
Links
- 238000000034 method Methods 0.000 title abstract 3
- GHBSPIPJMLAMEP-UHFFFAOYSA-N 6-pentyloxan-2-one Chemical class CCCCCC1CCCC(=O)O1 GHBSPIPJMLAMEP-UHFFFAOYSA-N 0.000 title 1
- KFSLWBXXFJQRDL-UHFFFAOYSA-N Peracetic acid Chemical compound CC(=O)OO KFSLWBXXFJQRDL-UHFFFAOYSA-N 0.000 abstract 2
- SCKXCAADGDQQCS-UHFFFAOYSA-N Performic acid Chemical compound OOC=O SCKXCAADGDQQCS-UHFFFAOYSA-N 0.000 abstract 2
- BGTOWKSIORTVQH-UHFFFAOYSA-N cyclopentanone Chemical compound O=C1CCCC1 BGTOWKSIORTVQH-UHFFFAOYSA-N 0.000 abstract 2
- IBXNCJKFFQIKKY-UHFFFAOYSA-N 1-pentyne Chemical compound CCCC#C IBXNCJKFFQIKKY-UHFFFAOYSA-N 0.000 abstract 1
- LJGHYPLBDBRCRZ-UHFFFAOYSA-N 3-(3-aminophenyl)sulfonylaniline Chemical compound NC1=CC=CC(S(=O)(=O)C=2C=C(N)C=CC=2)=C1 LJGHYPLBDBRCRZ-UHFFFAOYSA-N 0.000 abstract 1
- NWUSZZITHTZLFS-UHFFFAOYSA-N 5-hydroxydec-7-enoic acid Chemical compound CCC=CCC(O)CCCC(O)=O NWUSZZITHTZLFS-UHFFFAOYSA-N 0.000 abstract 1
- DOTXOHVZFKMFAE-UHFFFAOYSA-N 5-hydroxydec-7-ynoic acid Chemical compound OC(CCCC(=O)O)CC#CCC DOTXOHVZFKMFAE-UHFFFAOYSA-N 0.000 abstract 1
- KDLHZDBZIXYQEI-UHFFFAOYSA-N Palladium Chemical compound [Pd] KDLHZDBZIXYQEI-UHFFFAOYSA-N 0.000 abstract 1
- 125000001931 aliphatic group Chemical group 0.000 abstract 1
- 238000009903 catalytic hydrogenation reaction Methods 0.000 abstract 1
- 239000011981 lindlar catalyst Substances 0.000 abstract 1
- CZPZWMPYEINMCF-UHFFFAOYSA-N propaneperoxoic acid Chemical compound CCC(=O)OO CZPZWMPYEINMCF-UHFFFAOYSA-N 0.000 abstract 1
Classifications
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D315/00—Heterocyclic compounds containing rings having one oxygen atom as the only ring hetero atom according to more than one of groups C07D303/00 - C07D313/00
-
- C—CHEMISTRY; METALLURGY
- C11—ANIMAL OR VEGETABLE OILS, FATS, FATTY SUBSTANCES OR WAXES; FATTY ACIDS THEREFROM; DETERGENTS; CANDLES
- C11B—PRODUCING, e.g. BY PRESSING RAW MATERIALS OR BY EXTRACTION FROM WASTE MATERIALS, REFINING OR PRESERVING FATS, FATTY SUBSTANCES, e.g. LANOLIN, FATTY OILS OR WAXES; ESSENTIAL OILS; PERFUMES
- C11B9/00—Essential oils; Perfumes
- C11B9/0069—Heterocyclic compounds
- C11B9/0073—Heterocyclic compounds containing only O or S as heteroatoms
- C11B9/008—Heterocyclic compounds containing only O or S as heteroatoms the hetero rings containing six atoms
Landscapes
- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Life Sciences & Earth Sciences (AREA)
- Engineering & Computer Science (AREA)
- Chemical Kinetics & Catalysis (AREA)
- Oil, Petroleum & Natural Gas (AREA)
- Wood Science & Technology (AREA)
- Pyrane Compounds (AREA)
- Fats And Perfumes (AREA)
- Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)
- Low-Molecular Organic Synthesis Reactions Using Catalysts (AREA)
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
US67529267A | 1967-10-16 | 1967-10-16 |
Publications (1)
Publication Number | Publication Date |
---|---|
ES357649A1 true ES357649A1 (es) | 1970-03-16 |
Family
ID=24709844
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
ES357649A Expired ES357649A1 (es) | 1967-10-16 | 1968-08-29 | Un procedimiento para la producccion de una lactona insaturada. |
Country Status (7)
Country | Link |
---|---|
US (1) | US3531501A (enrdf_load_stackoverflow) |
BE (1) | BE721164A (enrdf_load_stackoverflow) |
CH (1) | CH507230A (enrdf_load_stackoverflow) |
ES (1) | ES357649A1 (enrdf_load_stackoverflow) |
FR (1) | FR1582339A (enrdf_load_stackoverflow) |
GB (1) | GB1205159A (enrdf_load_stackoverflow) |
NL (1) | NL6814210A (enrdf_load_stackoverflow) |
Families Citing this family (3)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
GB1594579A (en) * | 1976-12-23 | 1981-07-30 | Polak Frutal Works | Perfume compositions |
US4948905A (en) * | 1989-09-18 | 1990-08-14 | Iowa State University Reasearch Foundation, Inc. | Synthesis of vinyl lactones |
CN117304151A (zh) * | 2023-09-11 | 2023-12-29 | 安徽华业香料合肥有限公司 | 一种茉莉内酯的合成新方法 |
Family Cites Families (1)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US2362408A (en) * | 1941-06-14 | 1944-11-07 | Ciba Pharm Prod Inc | Lactones of the cyclopentano-poly-hydro-phenanthrene series and process of making same |
-
1967
- 1967-10-16 US US675292A patent/US3531501A/en not_active Expired - Lifetime
-
1968
- 1968-08-29 ES ES357649A patent/ES357649A1/es not_active Expired
- 1968-09-06 GB GB42559/68A patent/GB1205159A/en not_active Expired
- 1968-09-20 BE BE721164D patent/BE721164A/xx unknown
- 1968-09-23 FR FR1582339D patent/FR1582339A/fr not_active Expired
- 1968-10-04 NL NL6814210A patent/NL6814210A/xx unknown
- 1968-10-16 CH CH1549468A patent/CH507230A/de not_active IP Right Cessation
Also Published As
Publication number | Publication date |
---|---|
BE721164A (enrdf_load_stackoverflow) | 1969-03-03 |
US3531501A (en) | 1970-09-29 |
FR1582339A (enrdf_load_stackoverflow) | 1969-09-26 |
DE1803460B2 (de) | 1977-06-30 |
CH507230A (de) | 1971-05-15 |
DE1803460A1 (de) | 1969-05-08 |
GB1205159A (en) | 1970-09-16 |
NL6814210A (enrdf_load_stackoverflow) | 1969-04-18 |
Similar Documents
Publication | Publication Date | Title |
---|---|---|
GB1070323A (en) | Process for the preparation of epsilon-caprolactones | |
ES434712A1 (es) | Procedimiento para la preparacion de 2, 5-dimetil-3-(-2h)- furanona. | |
ES357649A1 (es) | Un procedimiento para la producccion de una lactona insaturada. | |
ES356738A1 (es) | Un aparato para hidrolizar compuestos de hidantoina. | |
ES288701A1 (es) | Procedimiento para la preparación de hidroxilamina | |
CH556191A (it) | Procedimento per la preparazione di catalizzatori adatti alla produzione dell'ossido di etilene mediante ossidazione dell' etilene. | |
FR2318149B1 (enrdf_load_stackoverflow) | ||
ES390599A1 (es) | Un procedimiento para la produccion de ciclohexano sustan- cialmente puro. | |
GB975715A (en) | A process for the preparation of solutions of pure percarboxylic acids | |
ES269394A1 (es) | Procedimiento para la preparacion de soluciones acuosas de acido paracético puro | |
ES288832A1 (es) | Procedimiento para la producción de cicloexilfenilcetona | |
GB1111543A (en) | Process for the preparation of ª†-lactones | |
GB917747A (en) | A method for the manufacture of glycerin | |
NL296871A (enrdf_load_stackoverflow) | ||
FR2244496A1 (en) | 4-(3-Chloro-4-cyclohexylphenyl)-gamma-butyrolactone - with analgesic and antiinflammatory activity | |
ES280036A1 (es) | Procedimiento de preparación de ácido exahidrobenzoico | |
FR2257339A1 (en) | Active chromium tricarboxylate catalyst - for reaction of cpds. contg. epoxyethane gps. with carboxylic acids or cyclicamides | |
ES434548A1 (es) | Procedimiento para preparar esteres de diglicidilo de aci- dos dicarboxilicos cicloalifaticos. | |
FR1022382A (fr) | Procédé de préparation d'un catalyseur de nickel très actif | |
GB1120257A (en) | Process for the production of 3,4-epoxysulpholane (3,4-epoxytetramethylenesulphone) | |
GB551990A (en) | Process for the manufacture of esters of pantothenic acid | |
GB1154066A (en) | Process for preparing 1-Amino-3-Carboxy-Propane-2-Sulfonic Acid | |
GB1341403A (en) | N-alkyl-n-3,4-methylenedioxyphenyl ureas | |
ES280754A1 (es) | Procedimiento de preparaciën de penicilina | |
GB951275A (en) | Process for the production of glycolic acid nitrile from methyl semiformal and hydrocyanic acid |