DE224844C - - Google Patents
Info
- Publication number
- DE224844C DE224844C DENDAT224844D DE224844DA DE224844C DE 224844 C DE224844 C DE 224844C DE NDAT224844 D DENDAT224844 D DE NDAT224844D DE 224844D A DE224844D A DE 224844DA DE 224844 C DE224844 C DE 224844C
- Authority
- DE
- Germany
- Prior art keywords
- acid
- crystallizes
- ethyl
- ether
- alcohol
- 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.)
- Active
Links
- 150000008064 anhydrides Chemical class 0.000 claims description 3
- 150000003870 salicylic acids Chemical class 0.000 claims description 3
- 125000000217 alkyl group Chemical group 0.000 claims description 2
- 150000003902 salicylic acid esters Chemical class 0.000 claims 1
- OKKJLVBELUTLKV-UHFFFAOYSA-N Methanol Chemical compound OC OKKJLVBELUTLKV-UHFFFAOYSA-N 0.000 description 15
- UHOVQNZJYSORNB-UHFFFAOYSA-N Benzene Chemical compound C1=CC=CC=C1 UHOVQNZJYSORNB-UHFFFAOYSA-N 0.000 description 12
- RTZKZFJDLAIYFH-UHFFFAOYSA-N Diethyl ether Chemical compound CCOCC RTZKZFJDLAIYFH-UHFFFAOYSA-N 0.000 description 12
- LFQSCWFLJHTTHZ-UHFFFAOYSA-N Ethanol Chemical compound CCO LFQSCWFLJHTTHZ-UHFFFAOYSA-N 0.000 description 6
- JUJWROOIHBZHMG-UHFFFAOYSA-N Pyridine Chemical compound C1=CC=NC=C1 JUJWROOIHBZHMG-UHFFFAOYSA-N 0.000 description 6
- 238000002844 melting Methods 0.000 description 4
- 230000008018 melting Effects 0.000 description 4
- HEMHJVSKTPXQMS-UHFFFAOYSA-M Sodium hydroxide Chemical compound [OH-].[Na+] HEMHJVSKTPXQMS-UHFFFAOYSA-M 0.000 description 3
- UMJSCPRVCHMLSP-UHFFFAOYSA-N pyridine Natural products COC1=CC=CN=C1 UMJSCPRVCHMLSP-UHFFFAOYSA-N 0.000 description 3
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 3
- CTNMSKKXHIFOQQ-UHFFFAOYSA-N 2-(3-phenylprop-2-enoyloxy)benzoic acid Chemical compound OC(=O)C1=CC=CC=C1OC(=O)C=CC1=CC=CC=C1 CTNMSKKXHIFOQQ-UHFFFAOYSA-N 0.000 description 2
- CSCPPACGZOOCGX-UHFFFAOYSA-N Acetone Chemical compound CC(C)=O CSCPPACGZOOCGX-UHFFFAOYSA-N 0.000 description 2
- BSYNRYMUTXBXSQ-UHFFFAOYSA-N Aspirin Chemical compound CC(=O)OC1=CC=CC=C1C(O)=O BSYNRYMUTXBXSQ-UHFFFAOYSA-N 0.000 description 2
- HEDRZPFGACZZDS-UHFFFAOYSA-N Chloroform Chemical compound ClC(Cl)Cl HEDRZPFGACZZDS-UHFFFAOYSA-N 0.000 description 2
- VEXZGXHMUGYJMC-UHFFFAOYSA-N Hydrochloric acid Chemical compound Cl VEXZGXHMUGYJMC-UHFFFAOYSA-N 0.000 description 2
- -1 acetylsalicylic acid carbonic acid ethyl ester Chemical compound 0.000 description 2
- 150000004651 carbonic acid esters Chemical class 0.000 description 2
- 150000001875 compounds Chemical class 0.000 description 2
- 238000001816 cooling Methods 0.000 description 2
- RIFGWPKJUGCATF-UHFFFAOYSA-N ethyl chloroformate Chemical compound CCOC(Cl)=O RIFGWPKJUGCATF-UHFFFAOYSA-N 0.000 description 2
- 239000000155 melt Substances 0.000 description 2
- 239000003921 oil Substances 0.000 description 2
- OAWXYINGQXLWOE-UHFFFAOYSA-N (2-acetyloxybenzoyl) 2-acetyloxybenzoate Chemical compound CC(=O)OC1=CC=CC=C1C(=O)OC(=O)C1=CC=CC=C1OC(C)=O OAWXYINGQXLWOE-UHFFFAOYSA-N 0.000 description 1
- QSOVSKMNRYAVJR-UHFFFAOYSA-N 2-benzoyloxybenzoic acid Chemical compound OC(=O)C1=CC=CC=C1OC(=O)C1=CC=CC=C1 QSOVSKMNRYAVJR-UHFFFAOYSA-N 0.000 description 1
- CNCMJNMYQXOHNN-UHFFFAOYSA-N 2-pentoxybenzoic acid Chemical compound CCCCCOC1=CC=CC=C1C(O)=O CNCMJNMYQXOHNN-UHFFFAOYSA-N 0.000 description 1
- QQAOCCOAMFWEDX-UHFFFAOYSA-N C(C1=CC=CC=C1)(=O)OC1=C(C(=O)O)C=CC=C1CC Chemical compound C(C1=CC=CC=C1)(=O)OC1=C(C(=O)O)C=CC=C1CC QQAOCCOAMFWEDX-UHFFFAOYSA-N 0.000 description 1
- HLDYXXYLUGPYEY-UHFFFAOYSA-N C(C1=CC=CC=C1)(=O)OC1=C(C(=O)OC(C2=C(C=CC=C2)OC(C2=CC=CC=C2)=O)=O)C=CC=C1 Chemical compound C(C1=CC=CC=C1)(=O)OC1=C(C(=O)OC(C2=C(C=CC=C2)OC(C2=CC=CC=C2)=O)=O)C=CC=C1 HLDYXXYLUGPYEY-UHFFFAOYSA-N 0.000 description 1
- FBGXZPVGXHQRCW-UHFFFAOYSA-N C(C=CC1=CC=CC=C1)(=O)OC1=C(C(=O)OC(C2=C(C=CC=C2)OC(C=CC2=CC=CC=C2)=O)=O)C=CC=C1 Chemical compound C(C=CC1=CC=CC=C1)(=O)OC1=C(C(=O)OC(C2=C(C=CC=C2)OC(C=CC2=CC=CC=C2)=O)=O)C=CC=C1 FBGXZPVGXHQRCW-UHFFFAOYSA-N 0.000 description 1
- UXVMQQNJUSDDNG-UHFFFAOYSA-L Calcium chloride Chemical compound [Cl-].[Cl-].[Ca+2] UXVMQQNJUSDDNG-UHFFFAOYSA-L 0.000 description 1
- BVKZGUZCCUSVTD-UHFFFAOYSA-L Carbonate Chemical compound [O-]C([O-])=O BVKZGUZCCUSVTD-UHFFFAOYSA-L 0.000 description 1
- CDBYLPFSWZWCQE-UHFFFAOYSA-L Sodium Carbonate Chemical compound [Na+].[Na+].[O-]C([O-])=O CDBYLPFSWZWCQE-UHFFFAOYSA-L 0.000 description 1
- 229940068372 acetyl salicylate Drugs 0.000 description 1
- 229960001138 acetylsalicylic acid Drugs 0.000 description 1
- 239000002253 acid Substances 0.000 description 1
- 150000007513 acids Chemical class 0.000 description 1
- ASGJEMPQQVNTGO-UHFFFAOYSA-N benzene chloroform Chemical compound C(Cl)(Cl)Cl.C1=CC=CC=C1.C1=CC=CC=C1 ASGJEMPQQVNTGO-UHFFFAOYSA-N 0.000 description 1
- 239000001110 calcium chloride Substances 0.000 description 1
- 229910001628 calcium chloride Inorganic materials 0.000 description 1
- 239000003814 drug Substances 0.000 description 1
- 238000001035 drying Methods 0.000 description 1
- 150000002148 esters Chemical class 0.000 description 1
- DYUMTASZJHGOHU-UHFFFAOYSA-N ethyl 2-benzoyloxybenzoate Chemical compound CCOC(=O)C1=CC=CC=C1OC(=O)C1=CC=CC=C1 DYUMTASZJHGOHU-UHFFFAOYSA-N 0.000 description 1
- 125000004494 ethyl ester group Chemical group 0.000 description 1
- 239000002244 precipitate Substances 0.000 description 1
- 235000021419 vinegar Nutrition 0.000 description 1
- 239000000052 vinegar Substances 0.000 description 1
Landscapes
- Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)
- Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
Publications (1)
| Publication Number | Publication Date |
|---|---|
| DE224844C true DE224844C (en:Method) |
Family
ID=485546
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| DENDAT224844D Active DE224844C (en:Method) |
Country Status (1)
| Country | Link |
|---|---|
| DE (1) | DE224844C (en:Method) |
Cited By (1)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US5475119A (en) * | 1991-12-21 | 1995-12-12 | Hoechst Aktiengesellschaft | Diallylammonium compounds, processes for their preparation and their use |
-
0
- DE DENDAT224844D patent/DE224844C/de active Active
Cited By (2)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US5475119A (en) * | 1991-12-21 | 1995-12-12 | Hoechst Aktiengesellschaft | Diallylammonium compounds, processes for their preparation and their use |
| US5563016A (en) * | 1991-12-21 | 1996-10-08 | Hoechst Ag | Diallylammonium compounds, processes for their preparation and their use |
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