SU191516A1 - - Google Patents
Info
- Publication number
- SU191516A1 SU191516A1 SU1065957A SU1065957A SU191516A1 SU 191516 A1 SU191516 A1 SU 191516A1 SU 1065957 A SU1065957 A SU 1065957A SU 1065957 A SU1065957 A SU 1065957A SU 191516 A1 SU191516 A1 SU 191516A1
- Authority
- SU
- USSR - Soviet Union
- Prior art keywords
- ether
- calculated
- found
- methyl
- bromide
- Prior art date
Links
- RTZKZFJDLAIYFH-UHFFFAOYSA-N Diethyl ether Chemical compound CCOCC RTZKZFJDLAIYFH-UHFFFAOYSA-N 0.000 description 15
- 239000000047 product Substances 0.000 description 5
- CSCPPACGZOOCGX-UHFFFAOYSA-N Acetone Chemical compound CC(C)=O CSCPPACGZOOCGX-UHFFFAOYSA-N 0.000 description 4
- VEXZGXHMUGYJMC-UHFFFAOYSA-N Hydrochloric acid Chemical compound Cl VEXZGXHMUGYJMC-UHFFFAOYSA-N 0.000 description 4
- QARVLSVVCXYDNA-UHFFFAOYSA-N bromobenzene Chemical compound BrC1=CC=CC=C1 QARVLSVVCXYDNA-UHFFFAOYSA-N 0.000 description 4
- CPELXLSAUQHCOX-UHFFFAOYSA-M Bromide Chemical compound [Br-] CPELXLSAUQHCOX-UHFFFAOYSA-M 0.000 description 3
- FYYHWMGAXLPEAU-UHFFFAOYSA-N Magnesium Chemical compound [Mg] FYYHWMGAXLPEAU-UHFFFAOYSA-N 0.000 description 3
- 125000000217 alkyl group Chemical group 0.000 description 3
- 238000009835 boiling Methods 0.000 description 3
- 229910052749 magnesium Inorganic materials 0.000 description 3
- 239000011777 magnesium Substances 0.000 description 3
- 238000000034 method Methods 0.000 description 3
- WHXSMMKQMYFTQS-UHFFFAOYSA-N Lithium Chemical compound [Li] WHXSMMKQMYFTQS-UHFFFAOYSA-N 0.000 description 2
- 238000006243 chemical reaction Methods 0.000 description 2
- 238000001816 cooling Methods 0.000 description 2
- 238000002474 experimental method Methods 0.000 description 2
- 150000002576 ketones Chemical class 0.000 description 2
- 229910052744 lithium Inorganic materials 0.000 description 2
- 241001137251 Corvidae Species 0.000 description 1
- KWYUFKZDYYNOTN-UHFFFAOYSA-M Potassium hydroxide Chemical compound [OH-].[K+] KWYUFKZDYYNOTN-UHFFFAOYSA-M 0.000 description 1
- 230000002378 acidificating effect Effects 0.000 description 1
- 150000001413 amino acids Chemical class 0.000 description 1
- 125000003118 aryl group Chemical group 0.000 description 1
- 230000015572 biosynthetic process Effects 0.000 description 1
- 239000007795 chemical reaction product Substances 0.000 description 1
- 150000001875 compounds Chemical class 0.000 description 1
- 125000000113 cyclohexyl group Chemical group [H]C1([H])C([H])([H])C([H])([H])C([H])(*)C([H])([H])C1([H])[H] 0.000 description 1
- 150000002148 esters Chemical class 0.000 description 1
- 239000000284 extract Substances 0.000 description 1
- 238000000605 extraction Methods 0.000 description 1
- 239000005457 ice water Substances 0.000 description 1
- 230000003993 interaction Effects 0.000 description 1
- INQOMBQAUSQDDS-UHFFFAOYSA-N iodomethane Chemical compound IC INQOMBQAUSQDDS-UHFFFAOYSA-N 0.000 description 1
- 238000004519 manufacturing process Methods 0.000 description 1
- -1 methyl acetylaminoethylcyclohexyl ketone Chemical compound 0.000 description 1
- 239000000203 mixture Substances 0.000 description 1
- 230000007935 neutral effect Effects 0.000 description 1
- 150000002894 organic compounds Chemical class 0.000 description 1
- 150000002901 organomagnesium compounds Chemical class 0.000 description 1
- ANRQGKOBLBYXFM-UHFFFAOYSA-M phenylmagnesium bromide Chemical compound Br[Mg]C1=CC=CC=C1 ANRQGKOBLBYXFM-UHFFFAOYSA-M 0.000 description 1
- 229940072033 potash Drugs 0.000 description 1
- BWHMMNNQKKPAPP-UHFFFAOYSA-L potassium carbonate Substances [K+].[K+].[O-]C([O-])=O BWHMMNNQKKPAPP-UHFFFAOYSA-L 0.000 description 1
- 235000015320 potassium carbonate Nutrition 0.000 description 1
- 238000002360 preparation method Methods 0.000 description 1
- 239000002994 raw material Substances 0.000 description 1
- 239000011541 reaction mixture Substances 0.000 description 1
- 229920006395 saturated elastomer Polymers 0.000 description 1
- 238000000926 separation method Methods 0.000 description 1
- 238000003756 stirring Methods 0.000 description 1
- 238000003786 synthesis reaction Methods 0.000 description 1
Publications (1)
Publication Number | Publication Date |
---|---|
SU191516A1 true SU191516A1 (enrdf_load_stackoverflow) |
Family
ID=
Similar Documents
Publication | Publication Date | Title |
---|---|---|
US2288211A (en) | Process for the production of betaalkoxyaldehydes | |
US4665219A (en) | Isolation of neopentyl glycol hydroxypivalate | |
SU191516A1 (enrdf_load_stackoverflow) | ||
SU492072A3 (ru) | Способ получени транс-хризантемовой кислоты | |
US5344975A (en) | Process for production of lower alkanoic acids | |
EP0093511B1 (en) | Method for producing and optically active 2,2-dimethylcyclopropanecarboxylic acid | |
JP2830210B2 (ja) | α,β―不飽和ケトン類の合成法 | |
US3046310A (en) | Oxenin intermediate and process for obtaining oxenin | |
Linstead et al. | CCLXVI.—Investigations of the olefinic acids. Part III. Homologues of teraconic, terebic, and pyroterebic acids. Further evidence of the effect of two γ-alkyl groups on three-carbon tautomerism | |
SU152467A1 (enrdf_load_stackoverflow) | ||
SU316689A1 (ru) | Способ получения | |
US2989555A (en) | Process for the preparation of epsilon-ketonic acids | |
US20040267040A1 (en) | Beta-ketophosphonates | |
SU271512A1 (ru) | Способ получения арилзамещенных этинилвиниловых эфиров | |
US2510364A (en) | Reaction of beta-lactones with organic magnesium halides | |
SU239968A1 (ru) | Способ получения замещенных тетрагидро-1-тиапи- ранонов-4 или октагидро-1-тиахроманонов-4 | |
SU352892A1 (ru) | Б ПОЛУЧЕНИЯ гомоизопилоповой кислоты | |
JP4294130B2 (ja) | α,β−不飽和ケトン化合物の製造方法 | |
US4965401A (en) | Process for the preparation of 2-propyl-2-pentenoic acid and its esters | |
DK158038B (da) | Fremgangsmaade til fremstilling af di-n-propylacetonitril | |
SU222367A1 (ru) | Способ получения алкилциклогексановой кислоты | |
SU239962A1 (ru) | Способ получения 4-алкоксипиримидо- | |
SU345132A1 (ru) | Способ получения сложных 7-хлорпропениловыхэфиров | |
SU429052A1 (ru) | СПОСОБ ПОЛУЧЕНИЯ КЕТАЛЕЙ СЛОЖНЫХ ЭФИРОВ а-КЕТОКИСЛОТ | |
US2425224A (en) | Process of obtaining thiodiglycolic acid |