GB858470A - Production of benzofurans - Google Patents
Production of benzofuransInfo
- Publication number
- GB858470A GB858470A GB3732358A GB3732358A GB858470A GB 858470 A GB858470 A GB 858470A GB 3732358 A GB3732358 A GB 3732358A GB 3732358 A GB3732358 A GB 3732358A GB 858470 A GB858470 A GB 858470A
- Authority
- GB
- United Kingdom
- Prior art keywords
- condensed
- give
- phenol
- hydroxyacetone
- methyl
- 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
- 150000001907 coumarones Chemical class 0.000 title abstract 2
- XLSMFKSTNGKWQX-UHFFFAOYSA-N hydroxyacetone Chemical compound CC(=O)CO XLSMFKSTNGKWQX-UHFFFAOYSA-N 0.000 abstract 8
- ISWSIDIOOBJBQZ-UHFFFAOYSA-N Phenol Chemical compound OC1=CC=CC=C1 ISWSIDIOOBJBQZ-UHFFFAOYSA-N 0.000 abstract 5
- GHMLBKRAJCXXBS-UHFFFAOYSA-N resorcinol Chemical compound OC1=CC=CC(O)=C1 GHMLBKRAJCXXBS-UHFFFAOYSA-N 0.000 abstract 4
- ROWKJAVDOGWPAT-UHFFFAOYSA-N Acetoin Chemical compound CC(O)C(C)=O ROWKJAVDOGWPAT-UHFFFAOYSA-N 0.000 abstract 2
- IJGRMHOSHXDMSA-UHFFFAOYSA-N Atomic nitrogen Chemical compound N#N IJGRMHOSHXDMSA-UHFFFAOYSA-N 0.000 abstract 2
- CURLTUGMZLYLDI-UHFFFAOYSA-N Carbon dioxide Chemical compound O=C=O CURLTUGMZLYLDI-UHFFFAOYSA-N 0.000 abstract 2
- XEEYBQQBJWHFJM-UHFFFAOYSA-N Iron Chemical compound [Fe] XEEYBQQBJWHFJM-UHFFFAOYSA-N 0.000 abstract 2
- 125000001931 aliphatic group Chemical group 0.000 abstract 2
- RDOXTESZEPMUJZ-UHFFFAOYSA-N anisole Chemical compound COC1=CC=CC=C1 RDOXTESZEPMUJZ-UHFFFAOYSA-N 0.000 abstract 2
- 150000001875 compounds Chemical class 0.000 abstract 2
- RWGFKTVRMDUZSP-UHFFFAOYSA-N cumene Chemical compound CC(C)C1=CC=CC=C1 RWGFKTVRMDUZSP-UHFFFAOYSA-N 0.000 abstract 2
- 238000000034 method Methods 0.000 abstract 2
- 150000002989 phenols Chemical class 0.000 abstract 2
- 239000002904 solvent Substances 0.000 abstract 2
- RYHBNJHYFVUHQT-UHFFFAOYSA-N 1,4-Dioxane Chemical compound C1COCCO1 RYHBNJHYFVUHQT-UHFFFAOYSA-N 0.000 abstract 1
- KJCVRFUGPWSIIH-UHFFFAOYSA-N 1-naphthol Chemical compound C1=CC=C2C(O)=CC=CC2=C1 KJCVRFUGPWSIIH-UHFFFAOYSA-N 0.000 abstract 1
- GJMIILRZDPIQPL-UHFFFAOYSA-N 2,3-dipropyl-1-benzofuran Chemical compound C1=CC=C2C(CCC)=C(CCC)OC2=C1 GJMIILRZDPIQPL-UHFFFAOYSA-N 0.000 abstract 1
- GBGPVUAOTCNZPT-UHFFFAOYSA-N 2-Methylcumarone Chemical compound C1=CC=C2OC(C)=CC2=C1 GBGPVUAOTCNZPT-UHFFFAOYSA-N 0.000 abstract 1
- DXMHWTUWSSJRID-UHFFFAOYSA-N 2-methyl-1-benzofuran-4-ol Chemical compound C1=CC=C2OC(C)=CC2=C1O DXMHWTUWSSJRID-UHFFFAOYSA-N 0.000 abstract 1
- CLBXCDSXUXNOIM-UHFFFAOYSA-N 3-oxidanylbutan-2-one Chemical compound CC(O)C(C)=O.CC(O)C(C)=O CLBXCDSXUXNOIM-UHFFFAOYSA-N 0.000 abstract 1
- BVEYJWQCMOVMAR-UHFFFAOYSA-N 5-Hydroxy-4-octanone Chemical compound CCCC(O)C(=O)CCC BVEYJWQCMOVMAR-UHFFFAOYSA-N 0.000 abstract 1
- RIZFJBAUFKFNKK-UHFFFAOYSA-N CCCC(O)C(=O)CCC.CCCC(O)C(=O)CCC Chemical compound CCCC(O)C(=O)CCC.CCCC(O)C(=O)CCC RIZFJBAUFKFNKK-UHFFFAOYSA-N 0.000 abstract 1
- UFHFLCQGNIYNRP-UHFFFAOYSA-N Hydrogen Chemical compound [H][H] UFHFLCQGNIYNRP-UHFFFAOYSA-N 0.000 abstract 1
- CTQNGGLPUBDAKN-UHFFFAOYSA-N O-Xylene Chemical compound CC1=CC=CC=C1C CTQNGGLPUBDAKN-UHFFFAOYSA-N 0.000 abstract 1
- 239000002253 acid Substances 0.000 abstract 1
- 150000007513 acids Chemical class 0.000 abstract 1
- 239000003513 alkali Substances 0.000 abstract 1
- 125000000217 alkyl group Chemical group 0.000 abstract 1
- PNEYBMLMFCGWSK-UHFFFAOYSA-N aluminium oxide Inorganic materials [O-2].[O-2].[O-2].[Al+3].[Al+3] PNEYBMLMFCGWSK-UHFFFAOYSA-N 0.000 abstract 1
- 229960000892 attapulgite Drugs 0.000 abstract 1
- 125000004432 carbon atom Chemical group C* 0.000 abstract 1
- 229910002092 carbon dioxide Inorganic materials 0.000 abstract 1
- 239000001569 carbon dioxide Substances 0.000 abstract 1
- 239000003054 catalyst Substances 0.000 abstract 1
- MVPPADPHJFYWMZ-UHFFFAOYSA-N chlorobenzene Chemical compound ClC1=CC=CC=C1 MVPPADPHJFYWMZ-UHFFFAOYSA-N 0.000 abstract 1
- 230000005494 condensation Effects 0.000 abstract 1
- 238000009833 condensation Methods 0.000 abstract 1
- 150000002170 ethers Chemical class 0.000 abstract 1
- 229910052739 hydrogen Inorganic materials 0.000 abstract 1
- 239000001257 hydrogen Substances 0.000 abstract 1
- 125000002887 hydroxy group Chemical group [H]O* 0.000 abstract 1
- GFAZHVHNLUBROE-UHFFFAOYSA-N hydroxymethyl propionaldehyde Natural products CCC(=O)CO GFAZHVHNLUBROE-UHFFFAOYSA-N 0.000 abstract 1
- 239000003701 inert diluent Substances 0.000 abstract 1
- 229910052500 inorganic mineral Inorganic materials 0.000 abstract 1
- 239000003456 ion exchange resin Substances 0.000 abstract 1
- 229920003303 ion-exchange polymer Polymers 0.000 abstract 1
- 229910052742 iron Inorganic materials 0.000 abstract 1
- 239000007791 liquid phase Substances 0.000 abstract 1
- UZKWTJUDCOPSNM-UHFFFAOYSA-N methoxybenzene Substances CCCCOC=C UZKWTJUDCOPSNM-UHFFFAOYSA-N 0.000 abstract 1
- 239000011707 mineral Substances 0.000 abstract 1
- 229910052757 nitrogen Inorganic materials 0.000 abstract 1
- RBXVOQPAMPBADW-UHFFFAOYSA-N nitrous acid;phenol Chemical class ON=O.OC1=CC=CC=C1 RBXVOQPAMPBADW-UHFFFAOYSA-N 0.000 abstract 1
- 229910052625 palygorskite Inorganic materials 0.000 abstract 1
- 239000012071 phase Substances 0.000 abstract 1
- 239000008262 pumice Substances 0.000 abstract 1
- 239000008096 xylene Substances 0.000 abstract 1
Classifications
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D307/00—Heterocyclic compounds containing five-membered rings having one oxygen atom as the only ring hetero atom
- C07D307/77—Heterocyclic compounds containing five-membered rings having one oxygen atom as the only ring hetero atom ortho- or peri-condensed with carbocyclic rings or ring systems
- C07D307/78—Benzo [b] furans; Hydrogenated benzo [b] furans
- C07D307/79—Benzo [b] furans; Hydrogenated benzo [b] furans with only hydrogen atoms, hydrocarbon or substituted hydrocarbon radicals, directly attached to carbon atoms of the hetero ring
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D307/00—Heterocyclic compounds containing five-membered rings having one oxygen atom as the only ring hetero atom
- C07D307/77—Heterocyclic compounds containing five-membered rings having one oxygen atom as the only ring hetero atom ortho- or peri-condensed with carbocyclic rings or ring systems
Landscapes
- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Furan Compounds (AREA)
Priority Applications (3)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
GB3732358A GB858470A (en) | 1958-11-20 | 1958-11-20 | Production of benzofurans |
FR809460A FR1239849A (fr) | 1958-11-20 | 1959-11-06 | Procédé de préparation de benzofuranes |
BE584743D BE584743A (enrdf_load_stackoverflow) | 1958-11-20 | 1959-11-17 |
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
GB3732358A GB858470A (en) | 1958-11-20 | 1958-11-20 | Production of benzofurans |
Publications (1)
Publication Number | Publication Date |
---|---|
GB858470A true GB858470A (en) | 1961-01-11 |
Family
ID=10395581
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
GB3732358A Expired GB858470A (en) | 1958-11-20 | 1958-11-20 | Production of benzofurans |
Country Status (3)
Country | Link |
---|---|
BE (1) | BE584743A (enrdf_load_stackoverflow) |
FR (1) | FR1239849A (enrdf_load_stackoverflow) |
GB (1) | GB858470A (enrdf_load_stackoverflow) |
-
1958
- 1958-11-20 GB GB3732358A patent/GB858470A/en not_active Expired
-
1959
- 1959-11-06 FR FR809460A patent/FR1239849A/fr not_active Expired
- 1959-11-17 BE BE584743D patent/BE584743A/xx unknown
Also Published As
Publication number | Publication date |
---|---|
BE584743A (enrdf_load_stackoverflow) | 1960-05-17 |
FR1239849A (fr) | 1960-08-26 |
Similar Documents
Publication | Publication Date | Title |
---|---|---|
US2468982A (en) | Preparation of bis-phenols | |
US3264358A (en) | Bisphenols | |
GB858470A (en) | Production of benzofurans | |
GB738359A (en) | Improvements in or relating to the preparation of aromatic hydroxy carboxylic acids and salts thereof | |
GB516936A (en) | Process for the manufacture of new reaction products from aromatic hydrocarbons | |
Chung et al. | Oxidative chlorination of phenols with hydrogen chloride/m-chloroperbenzoic acid/N, N-dimethylformamide system | |
GB923863A (en) | Improvements in or relating to branched polycarbonates | |
US3875247A (en) | Process for preparing alkylphenols by oxidising alkylbenzaldehydes | |
Entel | Nuclear Structure of the Water-soluble Polycarboxylic Acids from the Oxidation of Bituminous Coal: The Decarboxylation Reaction1 | |
GB979656A (en) | Process for the production of orthohydroxybenzyl alcohols | |
US2852568A (en) | Preparation of cycloalkadienyl derivatives of phenolic compounds | |
GB790644A (en) | Phenolic oxo-aldehyde resins | |
US3630855A (en) | Process for removing naphthalene from phenol by extractive distillation | |
US3076818A (en) | Production of benzofurans | |
GB842209A (en) | Preparation of bis(hydroxyphenyl)alkyl-methanes | |
GB770650A (en) | Improved process for the separation of aromatic isopropyl compounds from phenols | |
GB1043159A (en) | Process for preparing terpene phenolic resins | |
USRE31771E (en) | Process for the preparation of ortho-(hydrocarbylthio)-phenols | |
GB1307841A (en) | Process for the production of phenolic compounds | |
US3658920A (en) | Process for the production of phenols | |
BUU-HOÏ et al. | ALKYLATION OF PHENOLS AND NAPHTHOLS WITH SOME SYMMETRICAL TERTIARY ALCOHOLS | |
GB991223A (en) | Process for the production of n,n-di(hydroxyaryl) alkanes | |
GB803480A (en) | Improvements in or relating to the acid decomposition of organic hydroperoxides | |
GB979134A (en) | Improvements in or relating to the manufacture of phenols and alpha-alkyl styrenes | |
US3397235A (en) | Phenylhydrazino-propanethiols |