GB435336A - Process for the manufacture of cyclic ketones - Google Patents
Process for the manufacture of cyclic ketonesInfo
- Publication number
- GB435336A GB435336A GB17505/34A GB1750534A GB435336A GB 435336 A GB435336 A GB 435336A GB 17505/34 A GB17505/34 A GB 17505/34A GB 1750534 A GB1750534 A GB 1750534A GB 435336 A GB435336 A GB 435336A
- Authority
- GB
- United Kingdom
- Prior art keywords
- acid
- prepared
- groups
- cyanheptylic
- ethylaniline
- 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
- 150000003997 cyclic ketones Chemical class 0.000 title abstract 3
- 238000004519 manufacturing process Methods 0.000 title 1
- 238000000034 method Methods 0.000 title 1
- 239000002253 acid Substances 0.000 abstract 6
- OJGMBLNIHDZDGS-UHFFFAOYSA-N N-Ethylaniline Chemical compound CCNC1=CC=CC=C1 OJGMBLNIHDZDGS-UHFFFAOYSA-N 0.000 abstract 4
- KBQDZEMXPBDNGH-UHFFFAOYSA-N cycloheptadecanone Chemical compound O=C1CCCCCCCCCCCCCCCC1 KBQDZEMXPBDNGH-UHFFFAOYSA-N 0.000 abstract 4
- FYSNRJHAOHDILO-UHFFFAOYSA-N thionyl chloride Chemical compound ClS(Cl)=O FYSNRJHAOHDILO-UHFFFAOYSA-N 0.000 abstract 4
- RTZKZFJDLAIYFH-UHFFFAOYSA-N Diethyl ether Chemical compound CCOCC RTZKZFJDLAIYFH-UHFFFAOYSA-N 0.000 abstract 2
- UZBQIPPOMKBLAS-UHFFFAOYSA-N diethylazanide Chemical compound CC[N-]CC UZBQIPPOMKBLAS-UHFFFAOYSA-N 0.000 abstract 2
- DCAYPVUWAIABOU-UHFFFAOYSA-N hexadecane Chemical compound CCCCCCCCCCCCCCCC DCAYPVUWAIABOU-UHFFFAOYSA-N 0.000 abstract 2
- 125000004435 hydrogen atom Chemical group [H]* 0.000 abstract 2
- 229910052751 metal Inorganic materials 0.000 abstract 2
- 239000002184 metal Substances 0.000 abstract 2
- OJURWUUOVGOHJZ-UHFFFAOYSA-N methyl 2-[(2-acetyloxyphenyl)methyl-[2-[(2-acetyloxyphenyl)methyl-(2-methoxy-2-oxoethyl)amino]ethyl]amino]acetate Chemical compound C=1C=CC=C(OC(C)=O)C=1CN(CC(=O)OC)CCN(CC(=O)OC)CC1=CC=CC=C1OC(C)=O OJURWUUOVGOHJZ-UHFFFAOYSA-N 0.000 abstract 2
- NNFCIKHAZHQZJG-UHFFFAOYSA-N potassium cyanide Chemical compound [K+].N#[C-] NNFCIKHAZHQZJG-UHFFFAOYSA-N 0.000 abstract 2
- 239000000047 product Substances 0.000 abstract 2
- NGNBDVOYPDDBFK-UHFFFAOYSA-N 2-[2,4-di(pentan-2-yl)phenoxy]acetyl chloride Chemical compound CCCC(C)C1=CC=C(OCC(Cl)=O)C(C(C)CCC)=C1 NGNBDVOYPDDBFK-UHFFFAOYSA-N 0.000 abstract 1
- OCOAMRXJNIJKJS-UHFFFAOYSA-N 6-(n,2-dimethylanilino)-6-oxohexanoic acid Chemical compound OC(=O)CCCCC(=O)N(C)C1=CC=CC=C1C OCOAMRXJNIJKJS-UHFFFAOYSA-N 0.000 abstract 1
- SYJNIAYOJOFLMS-UHFFFAOYSA-N 8-(n,2-dimethylanilino)-8-oxooctanoic acid Chemical compound OC(=O)CCCCCCC(=O)N(C)C1=CC=CC=C1C SYJNIAYOJOFLMS-UHFFFAOYSA-N 0.000 abstract 1
- AEDUTIHKIQBFAN-UHFFFAOYSA-N C(C)NC1=CC=CC=C1.[Na] Chemical compound C(C)NC1=CC=CC=C1.[Na] AEDUTIHKIQBFAN-UHFFFAOYSA-N 0.000 abstract 1
- JFPFMDWCORUHNB-UHFFFAOYSA-N CNC1=CC=CC=C1.[K] Chemical compound CNC1=CC=CC=C1.[K] JFPFMDWCORUHNB-UHFFFAOYSA-N 0.000 abstract 1
- LNLCRJXCNQABMV-UHFFFAOYSA-N Dimethyl suberate Chemical compound COC(=O)CCCCCCC(=O)OC LNLCRJXCNQABMV-UHFFFAOYSA-N 0.000 abstract 1
- OFOBLEOULBTSOW-UHFFFAOYSA-N Malonic acid Chemical compound OC(=O)CC(O)=O OFOBLEOULBTSOW-UHFFFAOYSA-N 0.000 abstract 1
- QAOWNCQODCNURD-UHFFFAOYSA-N Sulfuric acid Chemical compound OS(O)(=O)=O QAOWNCQODCNURD-UHFFFAOYSA-N 0.000 abstract 1
- 125000002723 alicyclic group Chemical group 0.000 abstract 1
- 239000003513 alkali Substances 0.000 abstract 1
- 125000000217 alkyl group Chemical group 0.000 abstract 1
- 150000001409 amidines Chemical class 0.000 abstract 1
- 125000003710 aryl alkyl group Chemical group 0.000 abstract 1
- 125000003118 aryl group Chemical group 0.000 abstract 1
- 238000009835 boiling Methods 0.000 abstract 1
- 150000001732 carboxylic acid derivatives Chemical class 0.000 abstract 1
- 239000007795 chemical reaction product Substances 0.000 abstract 1
- 239000003795 chemical substances by application Substances 0.000 abstract 1
- 150000001875 compounds Chemical class 0.000 abstract 1
- 230000005494 condensation Effects 0.000 abstract 1
- 238000009833 condensation Methods 0.000 abstract 1
- CGZZMOTZOONQIA-UHFFFAOYSA-N cycloheptanone Chemical compound O=C1CCCCCC1 CGZZMOTZOONQIA-UHFFFAOYSA-N 0.000 abstract 1
- HPNMFZURTQLUMO-UHFFFAOYSA-N diethylamine Chemical compound CCNCC HPNMFZURTQLUMO-UHFFFAOYSA-N 0.000 abstract 1
- GGSUCNLOZRCGPQ-UHFFFAOYSA-N diethylaniline Chemical compound CCN(CC)C1=CC=CC=C1 GGSUCNLOZRCGPQ-UHFFFAOYSA-N 0.000 abstract 1
- 150000002148 esters Chemical class 0.000 abstract 1
- 125000004494 ethyl ester group Chemical group 0.000 abstract 1
- 229910052736 halogen Inorganic materials 0.000 abstract 1
- 150000002367 halogens Chemical class 0.000 abstract 1
- 238000010438 heat treatment Methods 0.000 abstract 1
- 125000001841 imino group Chemical group [H]N=* 0.000 abstract 1
- AHNJTQYTRPXLLG-UHFFFAOYSA-N lithium;diethylazanide Chemical compound [Li+].CC[N-]CC AHNJTQYTRPXLLG-UHFFFAOYSA-N 0.000 abstract 1
- XPVYVHOOOGLRDU-UHFFFAOYSA-N n-methylaniline;sodium Chemical compound [Na].CNC1=CC=CC=C1 XPVYVHOOOGLRDU-UHFFFAOYSA-N 0.000 abstract 1
- 125000002560 nitrile group Chemical group 0.000 abstract 1
- 125000002924 primary amino group Chemical group [H]N([H])* 0.000 abstract 1
- 238000007127 saponification reaction Methods 0.000 abstract 1
- ODZPKZBBUMBTMG-UHFFFAOYSA-N sodium amide Chemical compound [NH2-].[Na+] ODZPKZBBUMBTMG-UHFFFAOYSA-N 0.000 abstract 1
- 239000001117 sulphuric acid Substances 0.000 abstract 1
- 235000011149 sulphuric acid Nutrition 0.000 abstract 1
Classifications
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
- C07C45/00—Preparation of compounds having >C = O groups bound only to carbon or hydrogen atoms; Preparation of chelates of such compounds
- C07C45/42—Preparation of compounds having >C = O groups bound only to carbon or hydrogen atoms; Preparation of chelates of such compounds by hydrolysis
Landscapes
- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| DE435336X | 1933-06-13 |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| GB435336A true GB435336A (en) | 1935-09-19 |
Family
ID=6506754
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| GB17505/34A Expired GB435336A (en) | 1933-06-13 | 1934-06-13 | Process for the manufacture of cyclic ketones |
Country Status (2)
| Country | Link |
|---|---|
| BE (1) | BE403657A (enrdf_load_stackoverflow) |
| GB (1) | GB435336A (enrdf_load_stackoverflow) |
-
0
- BE BE403657D patent/BE403657A/xx unknown
-
1934
- 1934-06-13 GB GB17505/34A patent/GB435336A/en not_active Expired
Also Published As
| Publication number | Publication date |
|---|---|
| BE403657A (enrdf_load_stackoverflow) |
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