SU188511A1 - - Google Patents
Info
- Publication number
- SU188511A1 SU188511A1 SU1012303A SU1012303A SU188511A1 SU 188511 A1 SU188511 A1 SU 188511A1 SU 1012303 A SU1012303 A SU 1012303A SU 1012303 A SU1012303 A SU 1012303A SU 188511 A1 SU188511 A1 SU 188511A1
- Authority
- SU
- USSR - Soviet Union
- Prior art keywords
- mol
- furan
- dimethylaminomethyl
- yield
- paraform
- Prior art date
Links
- QTBSBXVTEAMEQO-UHFFFAOYSA-N Acetic acid Chemical compound CC(O)=O QTBSBXVTEAMEQO-UHFFFAOYSA-N 0.000 description 14
- WSFSSNUMVMOOMR-UHFFFAOYSA-N Formaldehyde Chemical compound O=C WSFSSNUMVMOOMR-UHFFFAOYSA-N 0.000 description 8
- 229920002866 paraformaldehyde Polymers 0.000 description 8
- 229960000583 acetic acid Drugs 0.000 description 7
- -1 dimethylaminomethyl-substituted furan Chemical class 0.000 description 7
- 239000012362 glacial acetic acid Substances 0.000 description 7
- YLQBMQCUIZJEEH-UHFFFAOYSA-N tetrahydrofuran Natural products C=1C=COC=1 YLQBMQCUIZJEEH-UHFFFAOYSA-N 0.000 description 7
- HEMHJVSKTPXQMS-UHFFFAOYSA-M Sodium hydroxide Chemical compound [OH-].[Na+] HEMHJVSKTPXQMS-UHFFFAOYSA-M 0.000 description 6
- VGIVLIHKENZQHQ-UHFFFAOYSA-N n,n,n',n'-tetramethylmethanediamine Chemical compound CN(C)CN(C)C VGIVLIHKENZQHQ-UHFFFAOYSA-N 0.000 description 6
- RTZKZFJDLAIYFH-UHFFFAOYSA-N Diethyl ether Chemical compound CCOCC RTZKZFJDLAIYFH-UHFFFAOYSA-N 0.000 description 4
- GSNUFIFRDBKVIE-UHFFFAOYSA-N 2,5-dimethylfuran Chemical compound CC1=CC=C(C)O1 GSNUFIFRDBKVIE-UHFFFAOYSA-N 0.000 description 3
- 238000000034 method Methods 0.000 description 3
- XFEBFJZELJVRQP-UHFFFAOYSA-N CC1=CC(=C(O1)C)CN(C)C Chemical compound CC1=CC(=C(O1)C)CN(C)C XFEBFJZELJVRQP-UHFFFAOYSA-N 0.000 description 2
- VEXZGXHMUGYJMC-UHFFFAOYSA-N Hydrochloric acid Chemical compound Cl VEXZGXHMUGYJMC-UHFFFAOYSA-N 0.000 description 2
- CSNNHWWHGAXBCP-UHFFFAOYSA-L Magnesium sulfate Chemical compound [Mg+2].[O-][S+2]([O-])([O-])[O-] CSNNHWWHGAXBCP-UHFFFAOYSA-L 0.000 description 2
- 238000004090 dissolution Methods 0.000 description 2
- 230000003993 interaction Effects 0.000 description 2
- 239000000203 mixture Substances 0.000 description 2
- 239000011541 reaction mixture Substances 0.000 description 2
- 235000011121 sodium hydroxide Nutrition 0.000 description 2
- VFIAOIVGTFADLM-UHFFFAOYSA-N 1-(furan-2-yl)-n,n-dimethylmethanamine Chemical compound CN(C)CC1=CC=CO1 VFIAOIVGTFADLM-UHFFFAOYSA-N 0.000 description 1
- VMMUZKSLBMOVHT-UHFFFAOYSA-N 1-[2-[(dimethylamino)methyl]furan-3-yl]-n,n-dimethylmethanamine Chemical compound CN(C)CC=1C=COC=1CN(C)C VMMUZKSLBMOVHT-UHFFFAOYSA-N 0.000 description 1
- FJSKXQVRKZTKSI-UHFFFAOYSA-N 2,3-dimethylfuran Chemical compound CC=1C=COC=1C FJSKXQVRKZTKSI-UHFFFAOYSA-N 0.000 description 1
- NYGVCCYPLJRCQS-UHFFFAOYSA-N 2-ethylsulfanyl-5-methylfuran Chemical compound C(C)SC=1OC(=CC1)C NYGVCCYPLJRCQS-UHFFFAOYSA-N 0.000 description 1
- 150000001412 amines Chemical class 0.000 description 1
- 238000001816 cooling Methods 0.000 description 1
- 125000006222 dimethylaminomethyl group Chemical group [H]C([H])([H])N(C([H])([H])[H])C([H])([H])* 0.000 description 1
- 239000012259 ether extract Substances 0.000 description 1
- 238000002474 experimental method Methods 0.000 description 1
- 229910052943 magnesium sulfate Inorganic materials 0.000 description 1
- 235000019341 magnesium sulphate Nutrition 0.000 description 1
- 238000004519 manufacturing process Methods 0.000 description 1
- 238000010992 reflux Methods 0.000 description 1
- 239000002904 solvent Substances 0.000 description 1
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 1
Publications (1)
Publication Number | Publication Date |
---|---|
SU188511A1 true SU188511A1 (enrdf_load_stackoverflow) |
Family
ID=
Similar Documents
Publication | Publication Date | Title |
---|---|---|
Hauser et al. | Condensations at the Methyl Group Rather than the Methylene Group of Benzoyl-and Acetylacetone Through Intermediate Dipotassio Salts1 | |
Newman et al. | The preparation of the six n-octynoic acids | |
Wawzonek et al. | The Formation of 4-chlorodibutylamine from N-chlorodibutylamine1 | |
SU188511A1 (enrdf_load_stackoverflow) | ||
SU457210A3 (ru) | Способ получени бензоил-/3-фенил/ -2-пропионовой или бензоил-/3-фенил/ -уксусной кислот | |
FR2803846A1 (fr) | 3-(1-hydroxy-pentylidene)-5-nitro-3h-benzofuran-2-one, son procede de preparation et son utilisation | |
Ramachandran et al. | Acetylation of Methyl Methoxycoumarilates and the Synthesis of 7-Methyl-9H-furo [3, 2-f][1] benzopyran-9-one1 | |
USRE31260E (en) | Process for the preparation of an acetonitrile derivative | |
US3287372A (en) | Process and intermediates for manufacture of 2-(dialkylmethyl)-5-alkyl-2-cyclohexen-1-ones | |
US4155929A (en) | Process for the preparation of an acetonitrile derivative | |
SU176306A1 (ru) | Способ получения 1-аренсульфонил- 2,2-диметилэтиленимидов | |
SU124447A1 (ru) | Способ получени 2-метил-а-тионафтенотиазола | |
SU194826A1 (ru) | Способ получения 3-бутил-5-ацетил-ы- -(|3-оксиэтил)пирролидона | |
SU181082A1 (enrdf_load_stackoverflow) | ||
Rockett et al. | The Catalytic Reduction of Dinitroneopentane | |
SU520907A3 (ru) | Способ получени замещенной бифенилилмасл ной кислоты или ее соли | |
SU251568A1 (ru) | СПОСОБ ПОЛУЧЕНИЯ а-МЕТИЛ-а-ОКСИ-р- НИТРОПРОПИОНОВОЙ КИСЛОТЫ | |
SU156656A1 (enrdf_load_stackoverflow) | ||
SU199864A1 (ru) | СПОСОБ ПОЛУЧЕНИЯ а-ЗАМЕЩЕННЫХ уБУТИРОЛАКТОН- Y-КАРБОНОВЫХ КИСЛОТ | |
SU250899A1 (ru) | ВСЬСГШЗЙАЯ in ПАТЕНТНО- ТЕХНИЧЕСКАЯ БИБЛИОТЕУЛ10 | |
SU283223A1 (ru) | СПОСОБ ПОЛУЧЕНИЯ N-(n-ФEHИЛAMИHOФEHИЛ)- МОРФОЛИНА | |
SU202130A1 (ru) | Способ получения фосфиноксида | |
US4515970A (en) | Process for preparation of alkanoic acids | |
SU198343A1 (ru) | Способ получения вторичных ароматических аминов | |
SU111907A1 (ru) | Способ получени 2,2-дифенил-4-диметил-аминопентанонитрила |