SU157970A1 - - Google Patents
Info
- Publication number
- SU157970A1 SU157970A1 SU778641A SU778641A SU157970A1 SU 157970 A1 SU157970 A1 SU 157970A1 SU 778641 A SU778641 A SU 778641A SU 778641 A SU778641 A SU 778641A SU 157970 A1 SU157970 A1 SU 157970A1
- Authority
- SU
- USSR - Soviet Union
- Prior art keywords
- ether
- calculated
- chloropentadiene
- dichloro
- found
- Prior art date
Links
- RTZKZFJDLAIYFH-UHFFFAOYSA-N Diethyl ether Chemical compound CCOCC RTZKZFJDLAIYFH-UHFFFAOYSA-N 0.000 description 13
- IJGRMHOSHXDMSA-UHFFFAOYSA-N Atomic nitrogen Chemical compound N#N IJGRMHOSHXDMSA-UHFFFAOYSA-N 0.000 description 4
- 239000000203 mixture Substances 0.000 description 4
- 239000000047 product Substances 0.000 description 4
- 238000004821 distillation Methods 0.000 description 3
- 230000007062 hydrolysis Effects 0.000 description 3
- 238000006460 hydrolysis reaction Methods 0.000 description 3
- LFQSCWFLJHTTHZ-UHFFFAOYSA-N Ethanol Chemical compound CCO LFQSCWFLJHTTHZ-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
- NBIIXXVUZAFLBC-UHFFFAOYSA-N Phosphoric acid Chemical compound OP(O)(O)=O NBIIXXVUZAFLBC-UHFFFAOYSA-N 0.000 description 2
- UIIMBOGNXHQVGW-UHFFFAOYSA-M Sodium bicarbonate Chemical compound [Na+].OC([O-])=O UIIMBOGNXHQVGW-UHFFFAOYSA-M 0.000 description 2
- FJKIXWOMBXYWOQ-UHFFFAOYSA-N ethenoxyethane Chemical compound CCOC=C FJKIXWOMBXYWOQ-UHFFFAOYSA-N 0.000 description 2
- 238000000034 method Methods 0.000 description 2
- 229910052757 nitrogen Inorganic materials 0.000 description 2
- 238000002360 preparation method Methods 0.000 description 2
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 2
- 229910021578 Iron(III) chloride Inorganic materials 0.000 description 1
- 235000008753 Papaver somniferum Nutrition 0.000 description 1
- 241000218180 Papaveraceae Species 0.000 description 1
- 101000579647 Penaeus vannamei Penaeidin-2a Proteins 0.000 description 1
- UIIMBOGNXHQVGW-DEQYMQKBSA-M Sodium bicarbonate-14C Chemical compound [Na+].O[14C]([O-])=O UIIMBOGNXHQVGW-DEQYMQKBSA-M 0.000 description 1
- 238000006243 chemical reaction Methods 0.000 description 1
- 150000001875 compounds Chemical class 0.000 description 1
- 239000007859 condensation product Substances 0.000 description 1
- 238000001816 cooling Methods 0.000 description 1
- 239000013078 crystal Substances 0.000 description 1
- 238000000354 decomposition reaction Methods 0.000 description 1
- RBTARNINKXHZNM-UHFFFAOYSA-K iron trichloride Chemical compound Cl[Fe](Cl)Cl RBTARNINKXHZNM-UHFFFAOYSA-K 0.000 description 1
- 229910052943 magnesium sulfate Inorganic materials 0.000 description 1
- 235000019341 magnesium sulphate Nutrition 0.000 description 1
- 239000003960 organic solvent Substances 0.000 description 1
- 239000003208 petroleum Substances 0.000 description 1
- 235000011007 phosphoric acid Nutrition 0.000 description 1
- 230000009257 reactivity Effects 0.000 description 1
- 238000001953 recrystallisation Methods 0.000 description 1
- 239000012047 saturated solution Substances 0.000 description 1
- 235000017557 sodium bicarbonate Nutrition 0.000 description 1
- 229910000030 sodium bicarbonate Inorganic materials 0.000 description 1
- 239000000243 solution Substances 0.000 description 1
- 239000007858 starting material Substances 0.000 description 1
- 238000003756 stirring Methods 0.000 description 1
- 235000014101 wine Nutrition 0.000 description 1
Publications (1)
Publication Number | Publication Date |
---|---|
SU157970A1 true SU157970A1 (enrdf_load_stackoverflow) |
Family
ID=
Similar Documents
Publication | Publication Date | Title |
---|---|---|
JP3841834B2 (ja) | マロン酸およびそのエステル | |
JPS6241702B2 (enrdf_load_stackoverflow) | ||
JPS6256481A (ja) | 6−メチル−3、4−ジヒドロ−1、2、3−オキサチアジン−4−オン−2、2−ジオキサイドの無毒性塩の製造方法 | |
US2525249A (en) | Making alkoxy isobutyric acids and derivatives thereof | |
SU157970A1 (enrdf_load_stackoverflow) | ||
US2456316A (en) | Method for producing alpha-ethylpiperonyl ethers | |
EP0075289A1 (en) | Process for making allylic esters of tetrabromophthalic acid | |
KR100330609B1 (ko) | 3-이속사졸카복실산의 제조방법 | |
US6087499A (en) | Process for producing 5-perfluoroalkyluracil derivatives | |
US2872461A (en) | Process of producing chloranil | |
US4414400A (en) | Process for the production of tetronic acid | |
CH395110A (de) | Procédé de préparation de la dibenzyloxyphosphorylcréatinine | |
US2844592A (en) | Preparation of conversion products of pentaerythrite dichlorohydrine monosulfurous acid esters | |
CN112745286B (zh) | 一种螺螨双酯衍生物的制备方法 | |
US4225714A (en) | Process for preparing p-chlorophenoxy-acetyl-piperonylpiperazine hydrochloride | |
JP2002047224A (ja) | 高純度ジトリメチロールプロパンの製造方法 | |
SU268423A1 (enrdf_load_stackoverflow) | ||
US2540307A (en) | 3, 4-diethoxymandelic acid and process for preparing same | |
JP4081619B2 (ja) | 光学活性な5−ヒドロキシ−2−デセン酸の製造方法および光学活性なマソイヤラクトンの製造方法 | |
US922538A (en) | Santalol esters. | |
US4172208A (en) | 5-Bromo-5,5-dicarboxyethylvalaraldehyde diethyl acetal | |
SU163621A1 (ru) | Способ получения циклосерина из эфиров серина | |
SU352871A1 (ru) | Способ получения гр?т-алкиловых эфиров ллкилфенолов | |
JPS5819665B2 (ja) | サクシニルコハクサンジエステルノ セイゾウホウ | |
US4433163A (en) | Process for the production of 3,3-dimethylglutaric acid or its esters |