NO115569B - - Google Patents
Download PDFInfo
- Publication number
- NO115569B NO115569B NO154322A NO15432264A NO115569B NO 115569 B NO115569 B NO 115569B NO 154322 A NO154322 A NO 154322A NO 15432264 A NO15432264 A NO 15432264A NO 115569 B NO115569 B NO 115569B
- Authority
- NO
- Norway
- Prior art keywords
- nitrophenyl
- ethyl acetate
- diol
- formula
- ethanol
- Prior art date
Links
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 claims description 11
- 238000000034 method Methods 0.000 claims description 10
- 230000007062 hydrolysis Effects 0.000 claims description 6
- 238000006460 hydrolysis reaction Methods 0.000 claims description 6
- 239000003795 chemical substances by application Substances 0.000 claims description 4
- 239000002253 acid Substances 0.000 claims description 3
- 150000001875 compounds Chemical class 0.000 claims description 3
- 150000001923 cyclic compounds Chemical class 0.000 claims description 3
- 239000003960 organic solvent Substances 0.000 claims description 3
- 238000002360 preparation method Methods 0.000 claims description 3
- 230000002378 acidificating effect Effects 0.000 claims description 2
- 150000008044 alkali metal hydroxides Chemical class 0.000 claims description 2
- 238000005904 alkaline hydrolysis reaction Methods 0.000 claims description 2
- 229910052736 halogen Inorganic materials 0.000 claims description 2
- 150000002367 halogens Chemical class 0.000 claims description 2
- 229910052739 hydrogen Inorganic materials 0.000 claims description 2
- 239000001257 hydrogen Substances 0.000 claims description 2
- 229910052500 inorganic mineral Inorganic materials 0.000 claims description 2
- 239000011707 mineral Substances 0.000 claims description 2
- DNIAPMSPPWPWGF-GSVOUGTGSA-N (R)-(-)-Propylene glycol Chemical compound C[C@@H](O)CO DNIAPMSPPWPWGF-GSVOUGTGSA-N 0.000 claims 1
- 238000005903 acid hydrolysis reaction Methods 0.000 claims 1
- 229910001854 alkali hydroxide Inorganic materials 0.000 claims 1
- 150000002431 hydrogen Chemical class 0.000 claims 1
- 239000002904 solvent Substances 0.000 claims 1
- XEKOWRVHYACXOJ-UHFFFAOYSA-N Ethyl acetate Chemical compound CCOC(C)=O XEKOWRVHYACXOJ-UHFFFAOYSA-N 0.000 description 81
- LFQSCWFLJHTTHZ-UHFFFAOYSA-N Ethanol Chemical compound CCO LFQSCWFLJHTTHZ-UHFFFAOYSA-N 0.000 description 41
- HEMHJVSKTPXQMS-UHFFFAOYSA-M Sodium hydroxide Chemical compound [OH-].[Na+] HEMHJVSKTPXQMS-UHFFFAOYSA-M 0.000 description 33
- VEXZGXHMUGYJMC-UHFFFAOYSA-N Hydrochloric acid Chemical compound Cl VEXZGXHMUGYJMC-UHFFFAOYSA-N 0.000 description 23
- 239000011541 reaction mixture Substances 0.000 description 15
- 239000000203 mixture Substances 0.000 description 12
- 239000000047 product Substances 0.000 description 12
- 125000004122 cyclic group Chemical group 0.000 description 9
- 239000000284 extract Substances 0.000 description 7
- OKKJLVBELUTLKV-UHFFFAOYSA-N Methanol Chemical compound OC OKKJLVBELUTLKV-UHFFFAOYSA-N 0.000 description 6
- LSNNMFCWUKXFEE-UHFFFAOYSA-N Sulfurous acid Chemical compound OS(O)=O LSNNMFCWUKXFEE-UHFFFAOYSA-N 0.000 description 6
- 238000004821 distillation Methods 0.000 description 5
- 238000001953 recrystallisation Methods 0.000 description 5
- RTZKZFJDLAIYFH-UHFFFAOYSA-N Diethyl ether Chemical compound CCOCC RTZKZFJDLAIYFH-UHFFFAOYSA-N 0.000 description 4
- 150000005676 cyclic carbonates Chemical class 0.000 description 4
- 230000004048 modification Effects 0.000 description 4
- 238000012986 modification Methods 0.000 description 4
- ZWEHNKRNPOVVGH-UHFFFAOYSA-N 2-Butanone Chemical compound CCC(C)=O ZWEHNKRNPOVVGH-UHFFFAOYSA-N 0.000 description 3
- CSCPPACGZOOCGX-UHFFFAOYSA-N Acetone Chemical compound CC(C)=O CSCPPACGZOOCGX-UHFFFAOYSA-N 0.000 description 3
- KWYUFKZDYYNOTN-UHFFFAOYSA-M Potassium hydroxide Chemical compound [OH-].[K+] KWYUFKZDYYNOTN-UHFFFAOYSA-M 0.000 description 3
- -1 benzoyl- Chemical class 0.000 description 3
- 239000000706 filtrate Substances 0.000 description 3
- LSNNMFCWUKXFEE-UHFFFAOYSA-L sulfite Chemical compound [O-]S([O-])=O LSNNMFCWUKXFEE-UHFFFAOYSA-L 0.000 description 3
- WSLDOOZREJYCGB-UHFFFAOYSA-N 1,2-Dichloroethane Chemical compound ClCCCl WSLDOOZREJYCGB-UHFFFAOYSA-N 0.000 description 2
- KFZMGEQAYNKOFK-UHFFFAOYSA-N Isopropanol Chemical compound CC(C)O KFZMGEQAYNKOFK-UHFFFAOYSA-N 0.000 description 2
- QAOWNCQODCNURD-UHFFFAOYSA-N Sulfuric acid Chemical compound OS(O)(=O)=O QAOWNCQODCNURD-UHFFFAOYSA-N 0.000 description 2
- 125000003236 benzoyl group Chemical group [H]C1=C([H])C([H])=C(C([H])=C1[H])C(*)=O 0.000 description 2
- 230000003115 biocidal effect Effects 0.000 description 2
- 125000004432 carbon atom Chemical group C* 0.000 description 2
- 238000002425 crystallisation Methods 0.000 description 2
- 230000008025 crystallization Effects 0.000 description 2
- 230000003287 optical effect Effects 0.000 description 2
- 239000003208 petroleum Substances 0.000 description 2
- 239000007858 starting material Substances 0.000 description 2
- 150000000185 1,3-diols Chemical class 0.000 description 1
- BMYNFMYTOJXKLE-UHFFFAOYSA-N 3-azaniumyl-2-hydroxypropanoate Chemical compound NCC(O)C(O)=O BMYNFMYTOJXKLE-UHFFFAOYSA-N 0.000 description 1
- YTBSYETUWUMLBZ-QWWZWVQMSA-N D-threose Chemical compound OC[C@@H](O)[C@H](O)C=O YTBSYETUWUMLBZ-QWWZWVQMSA-N 0.000 description 1
- 150000007513 acids Chemical class 0.000 description 1
- 125000002252 acyl group Chemical group 0.000 description 1
- 125000003545 alkoxy group Chemical group 0.000 description 1
- 235000011114 ammonium hydroxide Nutrition 0.000 description 1
- 238000009835 boiling Methods 0.000 description 1
- 238000006243 chemical reaction Methods 0.000 description 1
- KWGRBVOPPLSCSI-UHFFFAOYSA-N d-ephedrine Natural products CNC(C)C(O)C1=CC=CC=C1 KWGRBVOPPLSCSI-UHFFFAOYSA-N 0.000 description 1
- 150000002009 diols Chemical class 0.000 description 1
- 238000003810 ethyl acetate extraction Methods 0.000 description 1
- 125000001495 ethyl group Chemical group [H]C([H])([H])C([H])([H])* 0.000 description 1
- 238000010438 heat treatment Methods 0.000 description 1
- 125000004435 hydrogen atom Chemical class [H]* 0.000 description 1
- XLYOFNOQVPJJNP-UHFFFAOYSA-M hydroxide Chemical compound [OH-] XLYOFNOQVPJJNP-UHFFFAOYSA-M 0.000 description 1
- 239000002198 insoluble material Substances 0.000 description 1
- 239000000543 intermediate Substances 0.000 description 1
- 229960004592 isopropanol Drugs 0.000 description 1
- 238000004519 manufacturing process Methods 0.000 description 1
- JEUXZUSUYIHGNL-UHFFFAOYSA-N n,n-diethylethanamine;hydrate Chemical class O.CCN(CC)CC JEUXZUSUYIHGNL-UHFFFAOYSA-N 0.000 description 1
- 150000002894 organic compounds Chemical class 0.000 description 1
- 230000002035 prolonged effect Effects 0.000 description 1
- KWGRBVOPPLSCSI-WCBMZHEXSA-N pseudoephedrine Chemical compound CN[C@@H](C)[C@@H](O)C1=CC=CC=C1 KWGRBVOPPLSCSI-WCBMZHEXSA-N 0.000 description 1
- 229960003908 pseudoephedrine Drugs 0.000 description 1
- 125000001453 quaternary ammonium group Chemical group 0.000 description 1
- 239000000126 substance Substances 0.000 description 1
- BJAARRARQJZURR-UHFFFAOYSA-N trimethylazanium;hydroxide Chemical class O.CN(C)C BJAARRARQJZURR-UHFFFAOYSA-N 0.000 description 1
- 238000005292 vacuum distillation Methods 0.000 description 1
Classifications
-
- C—CHEMISTRY; METALLURGY
- C04—CEMENTS; CONCRETE; ARTIFICIAL STONE; CERAMICS; REFRACTORIES
- C04B—LIME, MAGNESIA; SLAG; CEMENTS; COMPOSITIONS THEREOF, e.g. MORTARS, CONCRETE OR LIKE BUILDING MATERIALS; ARTIFICIAL STONE; CERAMICS; REFRACTORIES; TREATMENT OF NATURAL STONE
- C04B22/00—Use of inorganic materials as active ingredients for mortars, concrete or artificial stone, e.g. accelerators or shrinkage compensating agents
-
- C—CHEMISTRY; METALLURGY
- C04—CEMENTS; CONCRETE; ARTIFICIAL STONE; CERAMICS; REFRACTORIES
- C04B—LIME, MAGNESIA; SLAG; CEMENTS; COMPOSITIONS THEREOF, e.g. MORTARS, CONCRETE OR LIKE BUILDING MATERIALS; ARTIFICIAL STONE; CERAMICS; REFRACTORIES; TREATMENT OF NATURAL STONE
- C04B7/00—Hydraulic cements
- C04B7/32—Aluminous cements
- C04B7/323—Calcium aluminosulfate cements, e.g. cements hydrating into ettringite
-
- Y—GENERAL TAGGING OF NEW TECHNOLOGICAL DEVELOPMENTS; GENERAL TAGGING OF CROSS-SECTIONAL TECHNOLOGIES SPANNING OVER SEVERAL SECTIONS OF THE IPC; TECHNICAL SUBJECTS COVERED BY FORMER USPC CROSS-REFERENCE ART COLLECTIONS [XRACs] AND DIGESTS
- Y02—TECHNOLOGIES OR APPLICATIONS FOR MITIGATION OR ADAPTATION AGAINST CLIMATE CHANGE
- Y02P—CLIMATE CHANGE MITIGATION TECHNOLOGIES IN THE PRODUCTION OR PROCESSING OF GOODS
- Y02P40/00—Technologies relating to the processing of minerals
- Y02P40/10—Production of cement, e.g. improving or optimising the production methods; Cement grinding
Landscapes
- Chemical & Material Sciences (AREA)
- Engineering & Computer Science (AREA)
- Ceramic Engineering (AREA)
- Materials Engineering (AREA)
- Structural Engineering (AREA)
- Organic Chemistry (AREA)
- Inorganic Chemistry (AREA)
- Curing Cements, Concrete, And Artificial Stone (AREA)
- Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
US30087463A | 1963-08-08 | 1963-08-08 |
Publications (1)
Publication Number | Publication Date |
---|---|
NO115569B true NO115569B (OSRAM) | 1968-10-21 |
Family
ID=23160957
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
NO154322A NO115569B (OSRAM) | 1963-08-08 | 1964-08-08 |
Country Status (8)
Country | Link |
---|---|
AT (1) | AT272927B (OSRAM) |
CH (1) | CH465478A (OSRAM) |
DE (2) | DE1302478B (OSRAM) |
ES (1) | ES302921A1 (OSRAM) |
GB (1) | GB1067858A (OSRAM) |
LU (1) | LU46722A1 (OSRAM) |
NL (1) | NL6409174A (OSRAM) |
NO (1) | NO115569B (OSRAM) |
Families Citing this family (4)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
DE4427661C2 (de) * | 1993-08-05 | 1999-08-26 | Denki Kagaku Kogyo Kk | Zementbeimischung, Zementzusammensetzung und Verwendung der Zementzusammensetzung |
MX9602271A (es) * | 1996-06-10 | 1998-04-30 | Cemex S A De C V | Cemento hidraulico con desarrollo acelerado de altas resistencias. |
DE19644654A1 (de) * | 1996-10-26 | 1998-04-30 | Kuzel Hans Juergen Prof Dr | Herstellung eines Sulfoaluminatzements aus aufbereiteten Salzschlacken |
WO2003035569A1 (fr) * | 2001-10-24 | 2003-05-01 | Boris Emmanuilovich Ioudovitch | Procede de production de ciment |
-
1964
- 1964-08-04 GB GB31632/64A patent/GB1067858A/en not_active Expired
- 1964-08-07 DE DEC33590A patent/DE1302478B/de active Pending
- 1964-08-07 CH CH1036264A patent/CH465478A/de unknown
- 1964-08-07 ES ES0302921A patent/ES302921A1/es not_active Expired
- 1964-08-07 LU LU46722D patent/LU46722A1/xx unknown
- 1964-08-07 AT AT681264A patent/AT272927B/de active
- 1964-08-07 DE DE19641471072 patent/DE1471072A1/de active Pending
- 1964-08-08 NO NO154322A patent/NO115569B/no unknown
- 1964-08-10 NL NL6409174A patent/NL6409174A/xx unknown
Also Published As
Publication number | Publication date |
---|---|
LU46722A1 (OSRAM) | 1964-10-29 |
GB1067858A (en) | 1967-05-03 |
AT272927B (de) | 1969-07-25 |
DE1471072A1 (de) | 1969-03-06 |
DE1302478B (de) | 1971-01-28 |
ES302921A1 (es) | 1965-02-16 |
NL6409174A (OSRAM) | 1965-02-09 |
CH465478A (de) | 1968-11-15 |
Similar Documents
Publication | Publication Date | Title |
---|---|---|
US2006114A (en) | Aliphatic-aromatic amine and process of making same | |
NO115569B (OSRAM) | ||
US1964973A (en) | 1 (3' 4' dioxyalkylene phenyl) 2 aminoalkanol (1) | |
IL38321A (en) | Lactones of 1'-alkyl-2,2'-alkylenedioxy-5'-hydroxy-4'-cyclopentenyl propionic acid | |
US2485146A (en) | Manufacture of chloro cresoxy acetic acid | |
US3796750A (en) | Process for the manufacture of pure l-n-benzoyl-3,4-dihydroxyphenylalanine | |
US2196580A (en) | Production of useful chemicals from isomeric mono - nitro - ortho - dichlorobenzene mixtures | |
US2695902A (en) | 2-methyl-3-(beta-chloroethyl)-4, 6-dichloro pyridine and method of making same | |
US2559011A (en) | Manufacture of n-allyl derivatives | |
DE905135C (de) | Verfahren zur Herstellung von N-Acylderivaten von 1-Nitrophenyl-2-aminopropan-1, 3-diolen | |
CH421963A (de) | Verfahren zur Herstellung von Aminoisoxazolen | |
US2732379A (en) | ||
US2116104A (en) | 3.5-dhodo-4-hydroxy acylophenone compounds and method for producing the same | |
DE1643463C3 (de) | Verfahren zur Herstellung von l-(p-Chlorbenzoyl>2-methyl-3-indolylessigsäuren | |
US2727063A (en) | Process for the preparation of optically active amino propane diols | |
SU511847A3 (ru) | Способ получени замещенной бифенилмасл ной кислоты или ее эфиров или солей | |
US2882292A (en) | Process for the production of 1-ketocyclo-octyl-2-acetic acid | |
US2464199A (en) | Alkylamino alkyl bromides | |
US2339083A (en) | Production of sulphathiazole | |
US2732375A (en) | Thebaine derivatives and process for | |
US3888871A (en) | Process for the preparation of 4-chloro-2-hydroxybenzothiazole | |
SU2699A1 (ru) | Способ получени кодеина | |
US1668964A (en) | Process for the manufacture of phenyl glycine or compounds thereof | |
US2074645A (en) | Pyrene compounds | |
NO853732L (no) | Fremgangsm¨te til fremstilling av pyrazolonderivater. |