NO134696B - - Google Patents
Download PDFInfo
- Publication number
- NO134696B NO134696B NO740371A NO740371A NO134696B NO 134696 B NO134696 B NO 134696B NO 740371 A NO740371 A NO 740371A NO 740371 A NO740371 A NO 740371A NO 134696 B NO134696 B NO 134696B
- Authority
- NO
- Norway
- Prior art keywords
- gold
- reaction
- iii
- acid
- trichloride
- Prior art date
Links
- 229910003803 Gold(III) chloride Inorganic materials 0.000 claims abstract description 14
- RJHLTVSLYWWTEF-UHFFFAOYSA-K gold trichloride Chemical compound Cl[Au](Cl)Cl RJHLTVSLYWWTEF-UHFFFAOYSA-K 0.000 claims abstract description 14
- 229940076131 gold trichloride Drugs 0.000 claims abstract description 12
- 238000000034 method Methods 0.000 claims abstract description 7
- 238000004519 manufacturing process Methods 0.000 claims abstract description 6
- 239000002253 acid Substances 0.000 claims description 8
- -1 tetrachlorogold(III) Chemical compound 0.000 claims description 8
- FYSNRJHAOHDILO-UHFFFAOYSA-N thionyl chloride Chemical compound ClS(Cl)=O FYSNRJHAOHDILO-UHFFFAOYSA-N 0.000 claims description 8
- 239000000203 mixture Substances 0.000 claims description 2
- 239000011541 reaction mixture Substances 0.000 claims description 2
- 238000006243 chemical reaction Methods 0.000 description 12
- WEVYAHXRMPXWCK-UHFFFAOYSA-N Acetonitrile Chemical compound CC#N WEVYAHXRMPXWCK-UHFFFAOYSA-N 0.000 description 8
- JUJWROOIHBZHMG-UHFFFAOYSA-N Pyridine Chemical compound C1=CC=NC=C1 JUJWROOIHBZHMG-UHFFFAOYSA-N 0.000 description 4
- 150000001875 compounds Chemical class 0.000 description 4
- 239000002904 solvent Substances 0.000 description 3
- ZAMOUSCENKQFHK-UHFFFAOYSA-N Chlorine atom Chemical compound [Cl] ZAMOUSCENKQFHK-UHFFFAOYSA-N 0.000 description 2
- IMNFDUFMRHMDMM-UHFFFAOYSA-N N-Heptane Chemical compound CCCCCCC IMNFDUFMRHMDMM-UHFFFAOYSA-N 0.000 description 2
- 239000000460 chlorine Substances 0.000 description 2
- 229910052801 chlorine Inorganic materials 0.000 description 2
- 238000001914 filtration Methods 0.000 description 2
- PCHJSUWPFVWCPO-UHFFFAOYSA-N gold Chemical compound [Au] PCHJSUWPFVWCPO-UHFFFAOYSA-N 0.000 description 2
- 239000010931 gold Substances 0.000 description 2
- 229910052737 gold Inorganic materials 0.000 description 2
- FDWREHZXQUYJFJ-UHFFFAOYSA-M gold monochloride Chemical compound [Cl-].[Au+] FDWREHZXQUYJFJ-UHFFFAOYSA-M 0.000 description 2
- 239000003446 ligand Substances 0.000 description 2
- IOLCXVTUBQKXJR-UHFFFAOYSA-M potassium bromide Chemical compound [K+].[Br-] IOLCXVTUBQKXJR-UHFFFAOYSA-M 0.000 description 2
- UMJSCPRVCHMLSP-UHFFFAOYSA-N pyridine Natural products COC1=CC=CN=C1 UMJSCPRVCHMLSP-UHFFFAOYSA-N 0.000 description 2
- 150000003839 salts Chemical class 0.000 description 2
- SDKPSXWGRWWLKR-UHFFFAOYSA-M sodium;9,10-dioxoanthracene-1-sulfonate Chemical compound [Na+].O=C1C2=CC=CC=C2C(=O)C2=C1C=CC=C2S(=O)(=O)[O-] SDKPSXWGRWWLKR-UHFFFAOYSA-M 0.000 description 2
- 230000003595 spectral effect Effects 0.000 description 2
- 239000007858 starting material Substances 0.000 description 2
- VEXZGXHMUGYJMC-UHFFFAOYSA-M Chloride anion Chemical compound [Cl-] VEXZGXHMUGYJMC-UHFFFAOYSA-M 0.000 description 1
- YGYAWVDWMABLBF-UHFFFAOYSA-N Phosgene Chemical compound ClC(Cl)=O YGYAWVDWMABLBF-UHFFFAOYSA-N 0.000 description 1
- 230000015572 biosynthetic process Effects 0.000 description 1
- 230000021523 carboxylation Effects 0.000 description 1
- 238000006473 carboxylation reaction Methods 0.000 description 1
- 239000003054 catalyst Substances 0.000 description 1
- 238000001704 evaporation Methods 0.000 description 1
- 230000008020 evaporation Effects 0.000 description 1
- 150000002334 glycols Chemical class 0.000 description 1
- 239000007787 solid Substances 0.000 description 1
- 238000005979 thermal decomposition reaction Methods 0.000 description 1
- 239000002023 wood Substances 0.000 description 1
Classifications
-
- C—CHEMISTRY; METALLURGY
- C01—INORGANIC CHEMISTRY
- C01G—COMPOUNDS CONTAINING METALS NOT COVERED BY SUBCLASSES C01D OR C01F
- C01G7/00—Compounds of gold
Landscapes
- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Inorganic Chemistry (AREA)
- Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)
- Catalysts (AREA)
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| IT20006/73A IT978790B (it) | 1973-02-05 | 1973-02-05 | Processo per la preparazione di tricloruro d oro anidro |
Publications (2)
| Publication Number | Publication Date |
|---|---|
| NO134696B true NO134696B (it) | 1976-08-23 |
| NO134696C NO134696C (it) | 1976-12-01 |
Family
ID=11163049
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| NO740371A NO134696C (it) | 1973-02-05 | 1974-02-05 |
Country Status (12)
| Country | Link |
|---|---|
| JP (1) | JPS5337833B2 (it) |
| BE (1) | BE810588A (it) |
| DE (1) | DE2405477C3 (it) |
| DK (1) | DK134812B (it) |
| FR (1) | FR2216229B1 (it) |
| GB (1) | GB1431632A (it) |
| IE (1) | IE38810B1 (it) |
| IT (1) | IT978790B (it) |
| LU (1) | LU69314A1 (it) |
| NL (1) | NL7401385A (it) |
| NO (1) | NO134696C (it) |
| ZA (1) | ZA74481B (it) |
-
1973
- 1973-02-05 IT IT20006/73A patent/IT978790B/it active
-
1974
- 1974-01-23 ZA ZA740481A patent/ZA74481B/xx unknown
- 1974-01-30 GB GB442574A patent/GB1431632A/en not_active Expired
- 1974-01-31 IE IE189/74A patent/IE38810B1/xx unknown
- 1974-01-31 NL NL7401385A patent/NL7401385A/xx not_active Application Discontinuation
- 1974-02-01 FR FR7403475A patent/FR2216229B1/fr not_active Expired
- 1974-02-04 BE BE140540A patent/BE810588A/xx unknown
- 1974-02-04 DK DK58774AA patent/DK134812B/da unknown
- 1974-02-04 LU LU69314A patent/LU69314A1/xx unknown
- 1974-02-05 NO NO740371A patent/NO134696C/no unknown
- 1974-02-05 JP JP1416774A patent/JPS5337833B2/ja not_active Expired
- 1974-02-05 DE DE2405477A patent/DE2405477C3/de not_active Expired
Also Published As
| Publication number | Publication date |
|---|---|
| IE38810L (en) | 1974-08-05 |
| FR2216229B1 (it) | 1976-06-25 |
| GB1431632A (en) | 1976-04-14 |
| IT978790B (it) | 1974-09-20 |
| ZA74481B (en) | 1974-11-27 |
| BE810588A (fr) | 1974-05-29 |
| LU69314A1 (it) | 1974-05-29 |
| DE2405477B2 (de) | 1975-03-13 |
| DE2405477A1 (de) | 1974-08-22 |
| NO134696C (it) | 1976-12-01 |
| IE38810B1 (en) | 1978-06-07 |
| DK134812C (it) | 1977-06-13 |
| FR2216229A1 (it) | 1974-08-30 |
| DE2405477C3 (de) | 1975-10-23 |
| JPS5337833B2 (it) | 1978-10-12 |
| NL7401385A (it) | 1974-08-07 |
| DK134812B (da) | 1977-01-24 |
| JPS49111896A (it) | 1974-10-24 |
Similar Documents
| Publication | Publication Date | Title |
|---|---|---|
| Yamasaki et al. | The Optical Resolution and Circular Dichroism of Cobalt (III) Complexes of the [Co (O–O) 2 (O–N)] 2− Type | |
| NO134696B (it) | ||
| SU554816A3 (ru) | Способ получени азотсодержащих полициклических соединений или их солей, или рацематов, или оптических антиподов | |
| US4024228A (en) | Process for the preparation of anhydrous gold trichloride | |
| JPS5949221B2 (ja) | 3−アシルアミノ−4−ホモイソツイスタンの製造法 | |
| US3321487A (en) | Organo aluminum compounds and method for obtaining them | |
| US2967859A (en) | Process for diglucose ureide | |
| CN110903211B (zh) | L-茶氨酸的制备方法 | |
| JP4833419B2 (ja) | 環式酸の製造 | |
| JP2773920B2 (ja) | テトラアンミンパラジウム(▲ii▼)クロライドの製造方法 | |
| US2710866A (en) | Process for preparing 2-amino-4-hydroxy-6-bromomethylpteridine | |
| Wade et al. | A convenient procedure for the conversion of monoorganomercury compounds, RHgX, to diorganomercurials | |
| CN110483360B (zh) | 一种阿法前列醇的合成方法 | |
| Pant et al. | Acetylenic derivatives of lead | |
| RU2810492C1 (ru) | Гидрат додекагидро-клозо-додекабората 2,4-диамин-6-фенил-1,3,5-триазина, способ его получения и применение в качестве осадительной формы B12H12 2--аниона | |
| SU673168A3 (ru) | Способ получени дигидрохлорида 2-оксиметил-3-окси-6-(1-окси-2-трет. бутиламиноэтил)пиридина | |
| JPS58194895A (ja) | DBc−AMP・Na塩の改良製造法 | |
| Connett et al. | Organomercury compounds. Part II. Preparations of complexes of bisperfluoroalkylmercurials by decarboxylation reactions | |
| Van der Wal et al. | Investigations in the vitamin B6‐series: I. synthesis of nor‐vitamin B6 | |
| US3912739A (en) | Aza-hydroxy-benzanthrone | |
| SU546616A1 (ru) | Способ получени 1н-2-оксопиридо /3,2-в/индолов | |
| RU2644356C1 (ru) | Способ получения спиро-гем-дихлорциклопропилмалонатов | |
| SU371237A1 (ru) | СПОСОБ ПОЛУЧЕНИЯ 5-ХЛОР-5,10-ДИГИДРОДИБЕНЗ- (Ь, е)-ФОСФОРИНА | |
| SU391062A1 (ru) | Способ получения двойного метаванадата калия | |
| CN117736139A (zh) | 一种吡啶-3-磺酰氯的合成方法 |