SU161739A1 - - Google Patents
Info
- Publication number
- SU161739A1 SU161739A1 SU827616A SU827616A SU161739A1 SU 161739 A1 SU161739 A1 SU 161739A1 SU 827616 A SU827616 A SU 827616A SU 827616 A SU827616 A SU 827616A SU 161739 A1 SU161739 A1 SU 161739A1
- Authority
- SU
- USSR - Soviet Union
- Prior art keywords
- mol
- magnesium
- aryl
- alkyl
- trichloride
- Prior art date
Links
- FYYHWMGAXLPEAU-UHFFFAOYSA-N Magnesium Chemical compound [Mg] FYYHWMGAXLPEAU-UHFFFAOYSA-N 0.000 claims description 7
- 229910052749 magnesium Inorganic materials 0.000 claims description 7
- 238000006243 chemical reaction Methods 0.000 claims description 6
- 239000011777 magnesium Substances 0.000 claims description 5
- 125000000217 alkyl group Chemical group 0.000 claims description 4
- 125000003118 aryl group Chemical group 0.000 claims description 4
- BMYNFMYTOJXKLE-UHFFFAOYSA-N 3-azaniumyl-2-hydroxypropanoate Chemical compound NCC(O)C(O)=O BMYNFMYTOJXKLE-UHFFFAOYSA-N 0.000 claims description 3
- 238000000034 method Methods 0.000 claims description 3
- 239000003960 organic solvent Substances 0.000 claims description 3
- 150000001412 amines Chemical class 0.000 claims description 2
- GDTBXPJZTBHREO-UHFFFAOYSA-N bromine Substances BrBr GDTBXPJZTBHREO-UHFFFAOYSA-N 0.000 claims description 2
- 229910052794 bromium Inorganic materials 0.000 claims description 2
- 125000001246 bromo group Chemical group Br* 0.000 claims description 2
- MOHQFYBUKQUPIQ-UHFFFAOYSA-N chloroarsane Chemical class [AsH2]Cl MOHQFYBUKQUPIQ-UHFFFAOYSA-N 0.000 claims description 2
- XMBWDFGMSWQBCA-UHFFFAOYSA-N hydrogen iodide Chemical compound I XMBWDFGMSWQBCA-UHFFFAOYSA-N 0.000 claims description 2
- 229940071870 hydroiodic acid Drugs 0.000 claims description 2
- 150000002900 organolithium compounds Chemical class 0.000 claims description 2
- 239000002994 raw material Substances 0.000 claims description 2
- 150000003335 secondary amines Chemical class 0.000 claims description 2
- 238000000926 separation method Methods 0.000 claims description 2
- 239000004475 Arginine Substances 0.000 claims 1
- ODKSFYDXXFIFQN-UHFFFAOYSA-N arginine Natural products OC(=O)C(N)CCCNC(N)=N ODKSFYDXXFIFQN-UHFFFAOYSA-N 0.000 claims 1
- UHOVQNZJYSORNB-UHFFFAOYSA-N Benzene Chemical compound C1=CC=CC=C1 UHOVQNZJYSORNB-UHFFFAOYSA-N 0.000 description 18
- RTZKZFJDLAIYFH-UHFFFAOYSA-N Diethyl ether Chemical compound CCOCC RTZKZFJDLAIYFH-UHFFFAOYSA-N 0.000 description 8
- 238000003756 stirring Methods 0.000 description 5
- IJGRMHOSHXDMSA-UHFFFAOYSA-N Atomic nitrogen Chemical compound N#N IJGRMHOSHXDMSA-UHFFFAOYSA-N 0.000 description 4
- 239000000203 mixture Substances 0.000 description 4
- JZBPFBNSONMJSJ-UHFFFAOYSA-N Cl.Cl.Cl.[AsH3] Chemical compound Cl.Cl.Cl.[AsH3] JZBPFBNSONMJSJ-UHFFFAOYSA-N 0.000 description 3
- VEXZGXHMUGYJMC-UHFFFAOYSA-N Hydrochloric acid Chemical compound Cl VEXZGXHMUGYJMC-UHFFFAOYSA-N 0.000 description 3
- KFZMGEQAYNKOFK-UHFFFAOYSA-N Isopropanol Chemical compound CC(C)O KFZMGEQAYNKOFK-UHFFFAOYSA-N 0.000 description 3
- 238000001816 cooling Methods 0.000 description 3
- KRHYYFGTRYWZRS-UHFFFAOYSA-N Fluorane Chemical compound F KRHYYFGTRYWZRS-UHFFFAOYSA-N 0.000 description 2
- MZRVEZGGRBJDDB-UHFFFAOYSA-N N-Butyllithium Chemical compound [Li]CCCC MZRVEZGGRBJDDB-UHFFFAOYSA-N 0.000 description 2
- OEYOHULQRFXULB-UHFFFAOYSA-N arsenic trichloride Chemical compound Cl[As](Cl)Cl OEYOHULQRFXULB-UHFFFAOYSA-N 0.000 description 2
- 230000015572 biosynthetic process Effects 0.000 description 2
- 238000009835 boiling Methods 0.000 description 2
- MVPPADPHJFYWMZ-UHFFFAOYSA-N chlorobenzene Chemical compound ClC1=CC=CC=C1 MVPPADPHJFYWMZ-UHFFFAOYSA-N 0.000 description 2
- 125000004177 diethyl group Chemical group [H]C([H])([H])C([H])([H])* 0.000 description 2
- HPNMFZURTQLUMO-UHFFFAOYSA-N diethylamine Chemical compound CCNCC HPNMFZURTQLUMO-UHFFFAOYSA-N 0.000 description 2
- 238000004821 distillation Methods 0.000 description 2
- 239000000706 filtrate Substances 0.000 description 2
- LWLPYZUDBNFNAH-UHFFFAOYSA-M magnesium;butane;bromide Chemical compound [Mg+2].[Br-].CCC[CH2-] LWLPYZUDBNFNAH-UHFFFAOYSA-M 0.000 description 2
- 238000004519 manufacturing process Methods 0.000 description 2
- 229910052757 nitrogen Inorganic materials 0.000 description 2
- 150000002901 organomagnesium compounds Chemical class 0.000 description 2
- 238000002360 preparation method Methods 0.000 description 2
- 239000000047 product Substances 0.000 description 2
- 239000002904 solvent Substances 0.000 description 2
- 238000003786 synthesis reaction Methods 0.000 description 2
- MPPPKRYCTPRNTB-UHFFFAOYSA-N 1-bromobutane Chemical compound CCCCBr MPPPKRYCTPRNTB-UHFFFAOYSA-N 0.000 description 1
- ZCYVEMRRCGMTRW-UHFFFAOYSA-N 7553-56-2 Chemical compound [I] ZCYVEMRRCGMTRW-UHFFFAOYSA-N 0.000 description 1
- UXVMQQNJUSDDNG-UHFFFAOYSA-L Calcium chloride Chemical compound [Cl-].[Cl-].[Ca+2] UXVMQQNJUSDDNG-UHFFFAOYSA-L 0.000 description 1
- 241001024304 Mino Species 0.000 description 1
- 229910001516 alkali metal iodide Inorganic materials 0.000 description 1
- 239000002585 base Substances 0.000 description 1
- -1 benzal Chemical class 0.000 description 1
- 150000001649 bromium compounds Chemical class 0.000 description 1
- DFGQSQUGJYNHRG-UHFFFAOYSA-N bromo(diphenyl)arsane Chemical compound C=1C=CC=CC=1[As](Br)C1=CC=CC=C1 DFGQSQUGJYNHRG-UHFFFAOYSA-N 0.000 description 1
- 235000010633 broth Nutrition 0.000 description 1
- KMGBZBJJOKUPIA-UHFFFAOYSA-N butyl iodide Chemical compound CCCCI KMGBZBJJOKUPIA-UHFFFAOYSA-N 0.000 description 1
- 239000001110 calcium chloride Substances 0.000 description 1
- 229910001628 calcium chloride Inorganic materials 0.000 description 1
- 238000000354 decomposition reaction Methods 0.000 description 1
- KYKXDTPUHIPKNG-UHFFFAOYSA-N dichloroarsane Chemical compound Cl[AsH]Cl KYKXDTPUHIPKNG-UHFFFAOYSA-N 0.000 description 1
- 230000003993 interaction Effects 0.000 description 1
- 229910052740 iodine Inorganic materials 0.000 description 1
- 239000011630 iodine Substances 0.000 description 1
- HJMSAAPFKZYBSQ-UHFFFAOYSA-M magnesium;butane;iodide Chemical compound [Mg+2].[I-].CCC[CH2-] HJMSAAPFKZYBSQ-UHFFFAOYSA-M 0.000 description 1
- 125000002496 methyl group Chemical group [H]C([H])([H])* 0.000 description 1
- 125000002347 octyl group Chemical group [H]C([*])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])[H] 0.000 description 1
- 239000012044 organic layer Substances 0.000 description 1
- 239000003208 petroleum Substances 0.000 description 1
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 1
Publications (1)
| Publication Number | Publication Date |
|---|---|
| SU161739A1 true SU161739A1 (enExample) |
Family
ID=
Similar Documents
| Publication | Publication Date | Title |
|---|---|---|
| US2862017A (en) | Benzyl esters of thiophosphoric acids and their production | |
| SU161739A1 (enExample) | ||
| CN111635431B (zh) | 一种苯基膦酸二苯酯的制备方法 | |
| CS207797B2 (en) | Method of making the derivatives of the clorstyrylpropan carboxyl acid | |
| JPH082914B2 (ja) | Ｏ，Ｏ−ジアルキル−γ−ホスホノーチグリン酸アルキルエステルの製法 | |
| Major et al. | a New Method for the Preparation of O, N-Dialkylhydroxylamines | |
| JP2004043405A (ja) | 高純度トリアリールホスフィンの工業的な製造法 | |
| SU156950A1 (enExample) | ||
| US3206516A (en) | Process for the production of 1, 4-dichloro hydrocarbons | |
| JPH0475224B2 (enExample) | ||
| SU199860A1 (enExample) | ||
| SU239327A1 (ru) | Способ получения циклодифосфазанов | |
| SU292985A1 (ru) | Способ получения тритиофосфонатов | |
| DK158038B (da) | Fremgangsmaade til fremstilling af di-n-propylacetonitril | |
| JP3073292B2 (ja) | ２，２，６，６−テトラメチル−４−オキソピペリジンの製造方法 | |
| JPS6312467B2 (enExample) | ||
| SU234393A1 (ru) | Способ получения алкилвинилгалоидов | |
| SU172323A1 (enExample) | ||
| SU441261A1 (ru) | Способ получени диорганодигалогенгерманов | |
| SU221702A1 (ru) | Способ получения нитротриалкил(арил)олова | |
| SU248688A1 (ru) | СПОСОБ ПОЛУЧЕНИЯ ХЛОРАНГИДРИДОВ 8-XИHOЛИH-N-(АРилсульФонил)-иминосульФиновых кислот | |
| SU341804A1 (ru) | Способ получения 1-галоид-1-тиоксофосфоленов | |
| SU221699A1 (ru) | Способ получения диэтилфосфатов ацилацетилметилкарбинолов | |
| RU2644356C1 (ru) | Способ получения спиро-гем-дихлорциклопропилмалонатов | |
| SU283218A1 (ru) | Способ получения стирилдифенилфосфина |