BE398150A - - Google Patents
Info
- Publication number
- BE398150A BE398150A BE398150DA BE398150A BE 398150 A BE398150 A BE 398150A BE 398150D A BE398150D A BE 398150DA BE 398150 A BE398150 A BE 398150A
- Authority
- BE
- Belgium
- Prior art keywords
- parts
- isatin
- water
- acid
- phenols
- Prior art date
Links
- 239000002253 acid Substances 0.000 claims description 6
- 238000000034 method Methods 0.000 claims description 6
- 150000002989 phenols Chemical class 0.000 claims description 5
- 241001465754 Metazoa Species 0.000 claims description 4
- 239000003795 chemical substances by application Substances 0.000 claims description 3
- 239000000835 fiber Substances 0.000 claims description 3
- 125000000217 alkyl group Chemical group 0.000 claims description 2
- 125000004432 carbon atom Chemical group C* 0.000 claims description 2
- 238000002360 preparation method Methods 0.000 claims description 2
- 241000894007 species Species 0.000 claims description 2
- 238000006467 substitution reaction Methods 0.000 claims description 2
- QPBDAHXYPMQZTA-UHFFFAOYSA-N 2,3-dioxoindole-1-sulfonic acid Chemical compound C1=CC=C2N(S(=O)(=O)O)C(=O)C(=O)C2=C1 QPBDAHXYPMQZTA-UHFFFAOYSA-N 0.000 claims 1
- QAOWNCQODCNURD-UHFFFAOYSA-N Sulfuric acid Chemical compound OS(O)(=O)=O QAOWNCQODCNURD-UHFFFAOYSA-N 0.000 description 12
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 11
- 239000007859 condensation product Substances 0.000 description 6
- UBHYCFBVIXOJJO-UHFFFAOYSA-N 2,3-dioxo-1h-indole-5-sulfonic acid Chemical compound OS(=O)(=O)C1=CC=C2NC(=O)C(=O)C2=C1 UBHYCFBVIXOJJO-UHFFFAOYSA-N 0.000 description 5
- JXDYKVIHCLTXOP-UHFFFAOYSA-N isatin Chemical compound C1=CC=C2C(=O)C(=O)NC2=C1 JXDYKVIHCLTXOP-UHFFFAOYSA-N 0.000 description 5
- WCUXLLCKKVVCTQ-UHFFFAOYSA-M Potassium chloride Chemical compound [Cl-].[K+] WCUXLLCKKVVCTQ-UHFFFAOYSA-M 0.000 description 4
- 238000006243 chemical reaction Methods 0.000 description 4
- BWHMMNNQKKPAPP-UHFFFAOYSA-L potassium carbonate Chemical compound [K+].[K+].[O-]C([O-])=O BWHMMNNQKKPAPP-UHFFFAOYSA-L 0.000 description 4
- 150000003839 salts Chemical class 0.000 description 4
- 159000000000 sodium salts Chemical class 0.000 description 4
- ISWSIDIOOBJBQZ-UHFFFAOYSA-N Phenol Chemical compound OC1=CC=CC=C1 ISWSIDIOOBJBQZ-UHFFFAOYSA-N 0.000 description 3
- HEMHJVSKTPXQMS-UHFFFAOYSA-M Sodium hydroxide Chemical compound [OH-].[Na+] HEMHJVSKTPXQMS-UHFFFAOYSA-M 0.000 description 3
- 230000002378 acidificating effect Effects 0.000 description 3
- 150000001875 compounds Chemical class 0.000 description 3
- 239000000203 mixture Substances 0.000 description 3
- 239000002244 precipitate Substances 0.000 description 3
- MEEKGULDSDXFCN-UHFFFAOYSA-N 2-pentylphenol Chemical compound CCCCCC1=CC=CC=C1O MEEKGULDSDXFCN-UHFFFAOYSA-N 0.000 description 2
- 238000009833 condensation Methods 0.000 description 2
- 230000005494 condensation Effects 0.000 description 2
- 238000004090 dissolution Methods 0.000 description 2
- QWVGKYWNOKOFNN-UHFFFAOYSA-N o-cresol Chemical compound CC1=CC=CC=C1O QWVGKYWNOKOFNN-UHFFFAOYSA-N 0.000 description 2
- 229910000027 potassium carbonate Inorganic materials 0.000 description 2
- 239000001103 potassium chloride Substances 0.000 description 2
- 235000011164 potassium chloride Nutrition 0.000 description 2
- 239000000843 powder Substances 0.000 description 2
- 239000000047 product Substances 0.000 description 2
- 238000003756 stirring Methods 0.000 description 2
- MGSRCZKZVOBKFT-UHFFFAOYSA-N thymol Chemical compound CC(C)C1=CC=C(C)C=C1O MGSRCZKZVOBKFT-UHFFFAOYSA-N 0.000 description 2
- JIAARYAFYJHUJI-UHFFFAOYSA-L zinc dichloride Chemical compound [Cl-].[Cl-].[Zn+2] JIAARYAFYJHUJI-UHFFFAOYSA-L 0.000 description 2
- SMFHPCZZAAMJJO-UHFFFAOYSA-N 2-chloro-5-methylphenol Chemical compound CC1=CC=C(Cl)C(O)=C1 SMFHPCZZAAMJJO-UHFFFAOYSA-N 0.000 description 1
- DOEKCDSLUSGPLD-UHFFFAOYSA-N 2-methyl-3-pentylphenol Chemical compound C(CCCC)C1=C(C(=CC=C1)O)C DOEKCDSLUSGPLD-UHFFFAOYSA-N 0.000 description 1
- WXNZTHHGJRFXKQ-UHFFFAOYSA-N 4-chlorophenol Chemical compound OC1=CC=C(Cl)C=C1 WXNZTHHGJRFXKQ-UHFFFAOYSA-N 0.000 description 1
- 241000238876 Acari Species 0.000 description 1
- 239000005844 Thymol Substances 0.000 description 1
- 229910021627 Tin(IV) chloride Inorganic materials 0.000 description 1
- 150000007513 acids Chemical class 0.000 description 1
- 239000003610 charcoal Substances 0.000 description 1
- 238000010411 cooking Methods 0.000 description 1
- 238000004821 distillation Methods 0.000 description 1
- 238000001914 filtration Methods 0.000 description 1
- 239000005457 ice water Substances 0.000 description 1
- 229910052500 inorganic mineral Inorganic materials 0.000 description 1
- 239000008141 laxative Substances 0.000 description 1
- 230000002475 laxative effect Effects 0.000 description 1
- 239000011707 mineral Substances 0.000 description 1
- 235000010755 mineral Nutrition 0.000 description 1
- 230000001766 physiological effect Effects 0.000 description 1
- 231100000614 poison Toxicity 0.000 description 1
- 230000007096 poisonous effect Effects 0.000 description 1
- XAEFZNCEHLXOMS-UHFFFAOYSA-M potassium benzoate Chemical compound [K+].[O-]C(=O)C1=CC=CC=C1 XAEFZNCEHLXOMS-UHFFFAOYSA-M 0.000 description 1
- 239000012264 purified product Substances 0.000 description 1
- 239000000126 substance Substances 0.000 description 1
- 229960000790 thymol Drugs 0.000 description 1
- HPGGPRDJHPYFRM-UHFFFAOYSA-J tin(iv) chloride Chemical compound Cl[Sn](Cl)(Cl)Cl HPGGPRDJHPYFRM-UHFFFAOYSA-J 0.000 description 1
- 238000005406 washing Methods 0.000 description 1
- 239000011592 zinc chloride Substances 0.000 description 1
- 235000005074 zinc chloride Nutrition 0.000 description 1
Landscapes
- Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)
Publications (1)
| Publication Number | Publication Date |
|---|---|
| BE398150A true BE398150A (https=) |
Family
ID=64719
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| BE398150D BE398150A (https=) |
Country Status (1)
| Country | Link |
|---|---|
| BE (1) | BE398150A (https=) |
-
0
- BE BE398150D patent/BE398150A/fr unknown
Similar Documents
| Publication | Publication Date | Title |
|---|---|---|
| Hilbert et al. | A study of the germicidal activity of diaryl-sulfide phenols | |
| BE398150A (https=) | ||
| Kaslow et al. | N-Substituted 4-Methylcarbostyrils1 | |
| Shirley et al. | Alkylation with Long Chain p-Toluenesulfonates. I. Alkylation of Phenols with n-Octadecyl p-Toluenesulfonate | |
| US2008337A (en) | Condensation product of dhsobutylene and polyhydric phenols | |
| Peak et al. | 89. Antituberculous compounds. Part IV. Compounds related to diethyl-ω-aryloxyalkylamines | |
| FR2612515A1 (fr) | Derives substitues de la benzidine, leur procede de fabrication et leur application dans le domaine therapeutique | |
| US2070353A (en) | Manufacture of isatin compounds | |
| Harding | CCLXII.—Substitution in aromatic hydroxy-compounds. Part II. Acetyl-nitro-substitution | |
| Wilson et al. | Rings Through the Meta and Para Positions of Benzene. a Study of Certain Ethers of Resorcinol and Meta-Aminophenol | |
| BE623104A (https=) | ||
| CH296185A (fr) | Procédé de préparation d'un nouveau dérivé de la phénothiazine. | |
| BE568504A (https=) | ||
| BE504017A (https=) | ||
| BE480430A (https=) | ||
| BE531131A (https=) | ||
| Morgan | LXXIV.—Action of formaldehyde on amines of the naphthalene series. Part II | |
| BE461878A (https=) | ||
| Griffith | The preparation of para-alkylphenols and para-alkylcatechols | |
| BE503014A (https=) | ||
| CH299944A (fr) | Procédé de préparation d'un dérivé de la pyrimidine. | |
| BE384788A (https=) | ||
| BE552488A (https=) | ||
| BE698702A (https=) | ||
| BE530534A (https=) |