ES250798A1 - UN PROCEDIMIENTO PARA PREPARAR COMPUESTOS ORGáNICOS HETEROCICLICOS - Google Patents
UN PROCEDIMIENTO PARA PREPARAR COMPUESTOS ORGáNICOS HETEROCICLICOSInfo
- Publication number
- ES250798A1 ES250798A1 ES0250798A ES250798A ES250798A1 ES 250798 A1 ES250798 A1 ES 250798A1 ES 0250798 A ES0250798 A ES 0250798A ES 250798 A ES250798 A ES 250798A ES 250798 A1 ES250798 A1 ES 250798A1
- Authority
- ES
- Spain
- Prior art keywords
- chloro
- methoxy
- halogen atom
- benzyl
- tetrahydro
- Prior art date
- Legal status (The legal status is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the status listed.)
- Expired
Links
- 238000000034 method Methods 0.000 title abstract 2
- CXWXQJXEFPUFDZ-UHFFFAOYSA-N tetralin Chemical class C1=CC=C2CCCCC2=C1 CXWXQJXEFPUFDZ-UHFFFAOYSA-N 0.000 title 1
- 125000005843 halogen group Chemical group 0.000 abstract 5
- 125000004435 hydrogen atom Chemical group [H]* 0.000 abstract 3
- 125000002887 hydroxy group Chemical group [H]O* 0.000 abstract 3
- IKHGUXGNUITLKF-UHFFFAOYSA-N Acetaldehyde Chemical compound CC=O IKHGUXGNUITLKF-UHFFFAOYSA-N 0.000 abstract 2
- 125000000217 alkyl group Chemical group 0.000 abstract 2
- 239000012280 lithium aluminium hydride Substances 0.000 abstract 2
- CTSLXHKWHWQRSH-UHFFFAOYSA-N oxalyl chloride Chemical compound ClC(=O)C(Cl)=O CTSLXHKWHWQRSH-UHFFFAOYSA-N 0.000 abstract 2
- FYSNRJHAOHDILO-UHFFFAOYSA-N thionyl chloride Chemical compound ClS(Cl)=O FYSNRJHAOHDILO-UHFFFAOYSA-N 0.000 abstract 2
- YPFDHNVEDLHUCE-UHFFFAOYSA-N 1,3-propanediol Substances OCCCO YPFDHNVEDLHUCE-UHFFFAOYSA-N 0.000 abstract 1
- FBMQNRKSAWNXBT-UHFFFAOYSA-N 1,4-diaminoanthracene-9,10-dione Chemical compound O=C1C2=CC=CC=C2C(=O)C2=C1C(N)=CC=C2N FBMQNRKSAWNXBT-UHFFFAOYSA-N 0.000 abstract 1
- SDGMUBWPXBSKCT-UHFFFAOYSA-N 1-chloro-4-methoxy-2-methylbenzene Chemical compound COC1=CC=C(Cl)C(C)=C1 SDGMUBWPXBSKCT-UHFFFAOYSA-N 0.000 abstract 1
- LTMRRSWNXVJMBA-UHFFFAOYSA-L 2,2-diethylpropanedioate Chemical compound CCC(CC)(C([O-])=O)C([O-])=O LTMRRSWNXVJMBA-UHFFFAOYSA-L 0.000 abstract 1
- TUSYWUYMMDEPDJ-UHFFFAOYSA-N 2-(1-methoxy-4-oxo-3H-naphthalen-2-yl)acetic acid Chemical compound COC1=C(CC(C2=CC=CC=C12)=O)CC(=O)O TUSYWUYMMDEPDJ-UHFFFAOYSA-N 0.000 abstract 1
- GHKLXXBWQJOXKB-UHFFFAOYSA-N 2-(bromomethyl)-1-chloro-4-methoxybenzene Chemical compound COC1=CC=C(Cl)C(CBr)=C1 GHKLXXBWQJOXKB-UHFFFAOYSA-N 0.000 abstract 1
- QHKFYKDZHMELQR-UHFFFAOYSA-N 3-benzylpentanedioic acid Chemical compound OC(=O)CC(CC(O)=O)CC1=CC=CC=C1 QHKFYKDZHMELQR-UHFFFAOYSA-N 0.000 abstract 1
- CPELXLSAUQHCOX-UHFFFAOYSA-M Bromide Chemical compound [Br-] CPELXLSAUQHCOX-UHFFFAOYSA-M 0.000 abstract 1
- PCLIMKBDDGJMGD-UHFFFAOYSA-N N-bromosuccinimide Chemical compound BrN1C(=O)CCC1=O PCLIMKBDDGJMGD-UHFFFAOYSA-N 0.000 abstract 1
- QAOWNCQODCNURD-UHFFFAOYSA-N Sulfuric acid Chemical compound OS(O)(=O)=O QAOWNCQODCNURD-UHFFFAOYSA-N 0.000 abstract 1
- WETWJCDKMRHUPV-UHFFFAOYSA-N acetyl chloride Chemical compound CC(Cl)=O WETWJCDKMRHUPV-UHFFFAOYSA-N 0.000 abstract 1
- 239000012346 acetyl chloride Substances 0.000 abstract 1
- 239000012445 acidic reagent Substances 0.000 abstract 1
- 150000008064 anhydrides Chemical class 0.000 abstract 1
- JFCQEDHGNNZCLN-UHFFFAOYSA-N anhydrous glutaric acid Natural products OC(=O)CCCC(O)=O JFCQEDHGNNZCLN-UHFFFAOYSA-N 0.000 abstract 1
- 125000004432 carbon atom Chemical group C* 0.000 abstract 1
- 238000010531 catalytic reduction reaction Methods 0.000 abstract 1
- 239000003795 chemical substances by application Substances 0.000 abstract 1
- -1 diethyl 2-chloro-5-methoxy-benzyl Chemical group 0.000 abstract 1
- 150000004820 halides Chemical class 0.000 abstract 1
- 229910052739 hydrogen Inorganic materials 0.000 abstract 1
- 239000001257 hydrogen Substances 0.000 abstract 1
- 230000003301 hydrolyzing effect Effects 0.000 abstract 1
- QARBMVPHQWIHKH-UHFFFAOYSA-N methanesulfonyl chloride Chemical compound CS(Cl)(=O)=O QARBMVPHQWIHKH-UHFFFAOYSA-N 0.000 abstract 1
- UHZYTMXLRWXGPK-UHFFFAOYSA-N phosphorus pentachloride Chemical compound ClP(Cl)(Cl)(Cl)Cl UHZYTMXLRWXGPK-UHFFFAOYSA-N 0.000 abstract 1
- 229920000166 polytrimethylene carbonate Polymers 0.000 abstract 1
- NNFCIKHAZHQZJG-UHFFFAOYSA-N potassium cyanide Chemical compound [K+].N#[C-] NNFCIKHAZHQZJG-UHFFFAOYSA-N 0.000 abstract 1
- 238000006722 reduction reaction Methods 0.000 abstract 1
- 238000006798 ring closing metathesis reaction Methods 0.000 abstract 1
- 239000001117 sulphuric acid Substances 0.000 abstract 1
- 235000011149 sulphuric acid Nutrition 0.000 abstract 1
Classifications
-
- C—CHEMISTRY; METALLURGY
- C21—METALLURGY OF IRON
- C21D—MODIFYING THE PHYSICAL STRUCTURE OF FERROUS METALS; GENERAL DEVICES FOR HEAT TREATMENT OF FERROUS OR NON-FERROUS METALS OR ALLOYS; MAKING METAL MALLEABLE, e.g. BY DECARBURISATION OR TEMPERING
- C21D1/00—General methods or devices for heat treatment, e.g. annealing, hardening, quenching or tempering
- C21D1/62—Quenching devices
- C21D1/63—Quenching devices for bath quenching
- C21D1/64—Quenching devices for bath quenching with circulating liquids
-
- C—CHEMISTRY; METALLURGY
- C09—DYES; PAINTS; POLISHES; NATURAL RESINS; ADHESIVES; COMPOSITIONS NOT OTHERWISE PROVIDED FOR; APPLICATIONS OF MATERIALS NOT OTHERWISE PROVIDED FOR
- C09B—ORGANIC DYES OR CLOSELY-RELATED COMPOUNDS FOR PRODUCING DYES, e.g. PIGMENTS; MORDANTS; LAKES
- C09B1/00—Dyes with anthracene nucleus not condensed with any other ring
- C09B1/16—Amino-anthraquinones
- C09B1/20—Preparation from starting materials already containing the anthracene nucleus
- C09B1/36—Dyes with acylated amino groups
- C09B1/40—Dyes with acylated amino groups the acyl groups being residues of an aliphatic or araliphatic carboxylic acid
Landscapes
- Chemical & Material Sciences (AREA)
- Engineering & Computer Science (AREA)
- Organic Chemistry (AREA)
- Physics & Mathematics (AREA)
- Thermal Sciences (AREA)
- Crystallography & Structural Chemistry (AREA)
- Mechanical Engineering (AREA)
- Materials Engineering (AREA)
- Metallurgy (AREA)
- Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| US74861358A | 1958-07-15 | 1958-07-15 |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| ES250798A1 true ES250798A1 (es) | 1959-12-16 |
Family
ID=25010184
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| ES0250798A Expired ES250798A1 (es) | 1958-07-15 | 1959-07-14 | UN PROCEDIMIENTO PARA PREPARAR COMPUESTOS ORGáNICOS HETEROCICLICOS |
Country Status (6)
| Country | Link |
|---|---|
| BE (1) | BE580716A (en, 2012) |
| CH (1) | CH393308A (en, 2012) |
| DE (1) | DE1111619B (en, 2012) |
| ES (1) | ES250798A1 (en, 2012) |
| GB (1) | GB917864A (en, 2012) |
| NL (1) | NL112821C (en, 2012) |
Family Cites Families (1)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| FR1098615A (fr) * | 1953-01-22 | 1955-08-16 | Philips Nv | Procédé de préparation d'alcools primaires de la série de la vitamine alpha |
-
0
- NL NL112821D patent/NL112821C/xx active
- BE BE580716D patent/BE580716A/xx unknown
-
1959
- 1959-07-14 CH CH7573959A patent/CH393308A/de unknown
- 1959-07-14 GB GB2413059A patent/GB917864A/en not_active Expired
- 1959-07-14 ES ES0250798A patent/ES250798A1/es not_active Expired
- 1959-07-15 DE DEA32480A patent/DE1111619B/de active Pending
Also Published As
| Publication number | Publication date |
|---|---|
| DE1111619B (de) | 1961-07-27 |
| CH393308A (de) | 1965-06-15 |
| BE580716A (en, 2012) | |
| GB917864A (en) | 1963-02-06 |
| NL112821C (en, 2012) |
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