SU285902A1 - - Google Patents
Info
- Publication number
- SU285902A1 SU285902A1 SU1046029A SU1046029A SU285902A1 SU 285902 A1 SU285902 A1 SU 285902A1 SU 1046029 A SU1046029 A SU 1046029A SU 1046029 A SU1046029 A SU 1046029A SU 285902 A1 SU285902 A1 SU 285902A1
- Authority
- SU
- USSR - Soviet Union
- Prior art keywords
- water
- dissolved
- solution
- added
- alcohol
- Prior art date
Links
- LFQSCWFLJHTTHZ-UHFFFAOYSA-N Ethanol Chemical compound CCO LFQSCWFLJHTTHZ-UHFFFAOYSA-N 0.000 description 9
- 239000000243 solution Substances 0.000 description 9
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 8
- 150000001413 amino acids Chemical class 0.000 description 5
- 235000019441 ethanol Nutrition 0.000 description 5
- UFHFLCQGNIYNRP-UHFFFAOYSA-N Hydrogen Chemical compound [H][H] UFHFLCQGNIYNRP-UHFFFAOYSA-N 0.000 description 4
- 239000007864 aqueous solution Substances 0.000 description 4
- 229910052739 hydrogen Inorganic materials 0.000 description 4
- 239000001257 hydrogen Substances 0.000 description 4
- 229910052751 metal Inorganic materials 0.000 description 4
- 239000002184 metal Substances 0.000 description 4
- 239000000203 mixture Substances 0.000 description 4
- 239000003054 catalyst Substances 0.000 description 3
- 238000005984 hydrogenation reaction Methods 0.000 description 3
- -1 palladium chlorides Chemical class 0.000 description 3
- 238000002360 preparation method Methods 0.000 description 3
- 108090000765 processed proteins & peptides Proteins 0.000 description 3
- 229910000033 sodium borohydride Inorganic materials 0.000 description 3
- 239000012279 sodium borohydride Substances 0.000 description 3
- XXROGKLTLUQVRX-UHFFFAOYSA-N allyl alcohol Chemical compound OCC=C XXROGKLTLUQVRX-UHFFFAOYSA-N 0.000 description 2
- 239000007795 chemical reaction product Substances 0.000 description 2
- 230000000694 effects Effects 0.000 description 2
- 238000000034 method Methods 0.000 description 2
- 102000004196 processed proteins & peptides Human genes 0.000 description 2
- BDERNNFJNOPAEC-UHFFFAOYSA-N propan-1-ol Chemical compound CCCO BDERNNFJNOPAEC-UHFFFAOYSA-N 0.000 description 2
- 229910052703 rhodium Inorganic materials 0.000 description 2
- 239000010948 rhodium Substances 0.000 description 2
- MHOVAHRLVXNVSD-UHFFFAOYSA-N rhodium atom Chemical compound [Rh] MHOVAHRLVXNVSD-UHFFFAOYSA-N 0.000 description 2
- 239000007858 starting material Substances 0.000 description 2
- KDYFGRWQOYBRFD-UHFFFAOYSA-N succinic acid group Chemical group C(CCC(=O)O)(=O)O KDYFGRWQOYBRFD-UHFFFAOYSA-N 0.000 description 2
- YNGDWRXWKFWCJY-UHFFFAOYSA-N 1,4-Dihydropyridine Chemical class C1C=CNC=C1 YNGDWRXWKFWCJY-UHFFFAOYSA-N 0.000 description 1
- OUYCCCASQSFEME-QMMMGPOBSA-N L-tyrosine Chemical compound OC(=O)[C@@H](N)CC1=CC=C(O)C=C1 OUYCCCASQSFEME-QMMMGPOBSA-N 0.000 description 1
- 238000010521 absorption reaction Methods 0.000 description 1
- 229910052783 alkali metal Inorganic materials 0.000 description 1
- 150000001340 alkali metals Chemical class 0.000 description 1
- MOOAHMCRPCTRLV-UHFFFAOYSA-N boron sodium Chemical compound [B].[Na] MOOAHMCRPCTRLV-UHFFFAOYSA-N 0.000 description 1
- 238000006243 chemical reaction Methods 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
- 238000004090 dissolution Methods 0.000 description 1
- 239000000706 filtrate Substances 0.000 description 1
- 229910052500 inorganic mineral Inorganic materials 0.000 description 1
- VZCYOOQTPOCHFL-UPHRSURJSA-N maleic acid Chemical compound OC(=O)\C=C/C(O)=O VZCYOOQTPOCHFL-UPHRSURJSA-N 0.000 description 1
- 150000002739 metals Chemical class 0.000 description 1
- 239000011707 mineral Substances 0.000 description 1
- 150000002894 organic compounds Chemical class 0.000 description 1
- 229910052763 palladium Inorganic materials 0.000 description 1
- KDLHZDBZIXYQEI-UHFFFAOYSA-N palladium Substances [Pd] KDLHZDBZIXYQEI-UHFFFAOYSA-N 0.000 description 1
- BASFCYQUMIYNBI-UHFFFAOYSA-N platinum Chemical group [Pt] BASFCYQUMIYNBI-UHFFFAOYSA-N 0.000 description 1
- 239000002244 precipitate Substances 0.000 description 1
- 239000000047 product Substances 0.000 description 1
- 239000001384 succinic acid Substances 0.000 description 1
- OUYCCCASQSFEME-UHFFFAOYSA-N tyrosine Natural products OC(=O)C(N)CC1=CC=C(O)C=C1 OUYCCCASQSFEME-UHFFFAOYSA-N 0.000 description 1
Publications (1)
| Publication Number | Publication Date |
|---|---|
| SU285902A1 true SU285902A1 (cs) |
Family
ID=
Similar Documents
| Publication | Publication Date | Title |
|---|---|---|
| BG51156A3 (bg) | Метод за получаване на n-метил-3(р-трифлуорметилфенокси)- 3-фенил-пропиламин хидрохлорид | |
| SU285902A1 (cs) | ||
| CN102336689A (zh) | 4-氯-3-(三氟甲基)苯磺酰氯的制备及其精制方法 | |
| US4073804A (en) | Producing glycine by the reductive amination of glyoxylic acid | |
| EP0253788B1 (en) | A method of preparing 5-amino salicyclic acid | |
| US3755194A (en) | Hydrogenation catalyst | |
| US4948890A (en) | Process for the preparation of DAFNP | |
| CN110963946A (zh) | 一种甲基牛磺酸钠的制备方法 | |
| CN114436864A (zh) | 一种2-甲基-5氨基苯酚的制备方法 | |
| SU679130A3 (ru) | Способ получени насышенных -аминокислот | |
| Hearon et al. | Chemicals from cellulose | |
| SU576937A3 (ru) | Способ получени моно- - оксиэтил-7-рутина | |
| SU259836A1 (ru) | Способ получения катализатора гидрирования | |
| CN109942441A (zh) | 一种间氨基苯酚的制备方法 | |
| SU207879A1 (ru) | Способ получения катализаторов гидрирования | |
| CN113582903B (zh) | 用l-2-氨基丁酰胺盐酸盐合成治疗癫痫病药物的方法 | |
| SU497296A1 (ru) | Способ получени производных 5,6-диаминопиримидинов | |
| SU154283A1 (cs) | ||
| EP0000634A1 (en) | Process for the manufacture of naphthylamine sulphonic acids | |
| US4299779A (en) | Catalytic reduction of 2-nitronaphthalene-4,8-disulfonic acid ammonium salt | |
| US4264526A (en) | Borate reduction of nitrophenols | |
| US3476801A (en) | Process for the preparation of methanylic acid | |
| SU255287A1 (ru) | Способ получения 1,4-диазобици'кло- | |
| JPS6039063B2 (ja) | ヒドロキシ酢酸の製造方法 | |
| SU173786A1 (cs) |