BE500843A - - Google Patents
Info
- Publication number
- BE500843A BE500843A BE500843DA BE500843A BE 500843 A BE500843 A BE 500843A BE 500843D A BE500843D A BE 500843DA BE 500843 A BE500843 A BE 500843A
- Authority
- BE
- Belgium
- Prior art keywords
- new chemical
- group
- page
- chloro
- chemical compound
- Prior art date
Links
- 238000000034 method Methods 0.000 claims description 8
- 150000001875 compounds Chemical class 0.000 claims description 7
- 125000001997 phenyl group Chemical group [H]C1=C([H])C([H])=C(*)C([H])=C1[H] 0.000 claims description 4
- 125000000217 alkyl group Chemical group 0.000 claims description 2
- 125000003277 amino group Chemical group 0.000 claims description 2
- 125000003118 aryl group Chemical group 0.000 claims description 2
- 238000006243 chemical reaction Methods 0.000 claims description 2
- 125000004093 cyano group Chemical group *C#N 0.000 claims description 2
- 229910052736 halogen Inorganic materials 0.000 claims description 2
- 150000002367 halogens Chemical class 0.000 claims description 2
- 125000003545 alkoxy group Chemical group 0.000 claims 1
- 150000001732 carboxylic acid derivatives Chemical class 0.000 claims 1
- RMXVHZFHSKRNJN-UHFFFAOYSA-N chlorourea Chemical compound NC(=O)NCl RMXVHZFHSKRNJN-UHFFFAOYSA-N 0.000 claims 1
- 239000000047 product Substances 0.000 description 10
- -1 AMINO Chemical class 0.000 description 7
- XNINAOUGJUYOQX-UHFFFAOYSA-M 2-cyanobutanoate Chemical compound CCC(C#N)C([O-])=O XNINAOUGJUYOQX-UHFFFAOYSA-M 0.000 description 6
- 239000003513 alkali Substances 0.000 description 5
- VEXZGXHMUGYJMC-UHFFFAOYSA-M chloride anion Chemical compound [Cl-] VEXZGXHMUGYJMC-UHFFFAOYSA-M 0.000 description 5
- 238000002844 melting Methods 0.000 description 5
- HEMHJVSKTPXQMS-UHFFFAOYSA-M sodium hydroxide Chemical compound [OH-].[Na+] HEMHJVSKTPXQMS-UHFFFAOYSA-M 0.000 description 4
- QTBSBXVTEAMEQO-UHFFFAOYSA-N acetic acid Chemical compound CC(O)=O QTBSBXVTEAMEQO-UHFFFAOYSA-N 0.000 description 3
- 239000002904 solvent Substances 0.000 description 3
- CSCPPACGZOOCGX-UHFFFAOYSA-N acetone Chemical compound CC(C)=O CSCPPACGZOOCGX-UHFFFAOYSA-N 0.000 description 2
- 239000002253 acid Substances 0.000 description 2
- UHOVQNZJYSORNB-UHFFFAOYSA-N benzene Chemical compound C1=CC=CC=C1 UHOVQNZJYSORNB-UHFFFAOYSA-N 0.000 description 2
- 239000003795 chemical substances by application Substances 0.000 description 2
- RTZKZFJDLAIYFH-UHFFFAOYSA-N diethyl ether Chemical compound CCOCC RTZKZFJDLAIYFH-UHFFFAOYSA-N 0.000 description 2
- 238000006460 hydrolysis reaction Methods 0.000 description 2
- 239000000203 mixture Substances 0.000 description 2
- 238000010992 reflux Methods 0.000 description 2
- 235000011121 sodium hydroxide Nutrition 0.000 description 2
- WQDUMFSSJAZKTM-UHFFFAOYSA-N sodium methoxide Chemical compound [Na+].[O-]C WQDUMFSSJAZKTM-UHFFFAOYSA-N 0.000 description 2
- HMTNYRXEKVKUJW-UHFFFAOYSA-N 2-chloro-4-(ethoxycarbonylamino)benzoic acid Chemical compound CCOC(=O)NC1=CC=C(C(O)=O)C(Cl)=C1 HMTNYRXEKVKUJW-UHFFFAOYSA-N 0.000 description 1
- IJJJSNBMFDDFBC-UHFFFAOYSA-N 2-cyanoethyl acetate Chemical compound CC(=O)OCCC#N IJJJSNBMFDDFBC-UHFFFAOYSA-N 0.000 description 1
- BEWGVKVWWKCFHO-UHFFFAOYSA-N 3-(4-aminophenyl)-3-oxopropanenitrile Chemical compound NC1=CC=C(C(=O)CC#N)C=C1 BEWGVKVWWKCFHO-UHFFFAOYSA-N 0.000 description 1
- JSYHLXLKPLAVSY-UHFFFAOYSA-N C(=O)(OCC)NC1=C(C(=O)Cl)C=C(C=C1)Cl Chemical compound C(=O)(OCC)NC1=C(C(=O)Cl)C=C(C=C1)Cl JSYHLXLKPLAVSY-UHFFFAOYSA-N 0.000 description 1
- PBIPPZUEMBAORX-UHFFFAOYSA-N C(=O)(OCC)NC=1C=C(C(=O)Cl)C=CC1Cl Chemical compound C(=O)(OCC)NC=1C=C(C(=O)Cl)C=CC1Cl PBIPPZUEMBAORX-UHFFFAOYSA-N 0.000 description 1
- NGCNIJJTRNKHFU-UHFFFAOYSA-N C(=O)(OCC)NC=1C=C(C(=O)Cl)C=CC1OC1=CC=CC=C1 Chemical compound C(=O)(OCC)NC=1C=C(C(=O)Cl)C=CC1OC1=CC=CC=C1 NGCNIJJTRNKHFU-UHFFFAOYSA-N 0.000 description 1
- KOGMTRHOEOGUKK-UHFFFAOYSA-N CC1=C(C(=O)Cl)C=CC(=C1)NC(=O)OCC Chemical compound CC1=C(C(=O)Cl)C=CC(=C1)NC(=O)OCC KOGMTRHOEOGUKK-UHFFFAOYSA-N 0.000 description 1
- MZRNXVAXTUMGOU-UHFFFAOYSA-N COC1=C(C(=O)CC#N)C=C(C(=C1)N)OC Chemical compound COC1=C(C(=O)CC#N)C=C(C(=C1)N)OC MZRNXVAXTUMGOU-UHFFFAOYSA-N 0.000 description 1
- WPRGBADDWICPEG-UHFFFAOYSA-N ClC1=C(C(=O)CC#N)C=CC(=C1)N Chemical compound ClC1=C(C(=O)CC#N)C=CC(=C1)N WPRGBADDWICPEG-UHFFFAOYSA-N 0.000 description 1
- 238000005727 Friedel-Crafts reaction Methods 0.000 description 1
- VEXZGXHMUGYJMC-UHFFFAOYSA-N HCl Chemical compound Cl VEXZGXHMUGYJMC-UHFFFAOYSA-N 0.000 description 1
- KOMVJUXSDIVWKW-UHFFFAOYSA-N O(C1=CC=CC=C1)NC1=CC=C(C(=O)CC#N)C=C1 Chemical compound O(C1=CC=CC=C1)NC1=CC=C(C(=O)CC#N)C=C1 KOMVJUXSDIVWKW-UHFFFAOYSA-N 0.000 description 1
- WEVYAHXRMPXWCK-UHFFFAOYSA-N acetonitrile Chemical class CC#N WEVYAHXRMPXWCK-UHFFFAOYSA-N 0.000 description 1
- 125000005001 aminoaryl group Chemical group 0.000 description 1
- ZJRCIQAMTAINCB-UHFFFAOYSA-N benzoylacetonitrile Chemical compound N#CCC(=O)C1=CC=CC=C1 ZJRCIQAMTAINCB-UHFFFAOYSA-N 0.000 description 1
- 239000003153 chemical reaction reagent Substances 0.000 description 1
- 238000001816 cooling Methods 0.000 description 1
- 238000005837 enolization reaction Methods 0.000 description 1
- IXCSERBJSXMMFS-UHFFFAOYSA-N hydrogen chloride Substances Cl.Cl IXCSERBJSXMMFS-UHFFFAOYSA-N 0.000 description 1
- 229910000041 hydrogen chloride Inorganic materials 0.000 description 1
- 239000012442 inert solvent Substances 0.000 description 1
- 239000000155 melt Substances 0.000 description 1
- 239000003208 petroleum Substances 0.000 description 1
- 125000000951 phenoxy group Chemical group [H]C1=C([H])C([H])=C(O*)C([H])=C1[H] 0.000 description 1
- 239000002244 precipitate Substances 0.000 description 1
- KEAYESYHFKHZAL-UHFFFAOYSA-N sodium Chemical compound [Na] KEAYESYHFKHZAL-UHFFFAOYSA-N 0.000 description 1
- 229910052708 sodium Inorganic materials 0.000 description 1
- 239000011734 sodium Substances 0.000 description 1
- 238000003756 stirring Methods 0.000 description 1
- 239000000126 substance Substances 0.000 description 1
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 1
Classifications
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
- C07C255/00—Carboxylic acid nitriles
Landscapes
- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)
Publications (1)
| Publication Number | Publication Date |
|---|---|
| BE500843A true BE500843A (de) |
Family
ID=142826
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| BE500843D BE500843A (de) |
Country Status (1)
| Country | Link |
|---|---|
| BE (1) | BE500843A (de) |
-
0
- BE BE500843D patent/BE500843A/fr unknown
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