GB1227601A - - Google Patents
Info
- Publication number
- GB1227601A GB1227601A GB1227601DA GB1227601A GB 1227601 A GB1227601 A GB 1227601A GB 1227601D A GB1227601D A GB 1227601DA GB 1227601 A GB1227601 A GB 1227601A
- Authority
- GB
- United Kingdom
- Prior art keywords
- butanol
- alcohols
- group
- crotonaldehyde
- butyraldehyde
- 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
- DKPFZGUDAPQIHT-UHFFFAOYSA-N Butyl acetate Natural products CCCCOC(C)=O DKPFZGUDAPQIHT-UHFFFAOYSA-N 0.000 abstract 6
- LRHPLDYGYMQRHN-UHFFFAOYSA-N N-Butanol Chemical compound CCCCO LRHPLDYGYMQRHN-UHFFFAOYSA-N 0.000 abstract 5
- ZTQSAGDEMFDKMZ-UHFFFAOYSA-N Butyraldehyde Chemical compound CCCC=O ZTQSAGDEMFDKMZ-UHFFFAOYSA-N 0.000 abstract 4
- XYFCBTPGUUZFHI-UHFFFAOYSA-N phosphine group Chemical group P XYFCBTPGUUZFHI-UHFFFAOYSA-N 0.000 abstract 4
- WVDDGKGOMKODPV-UHFFFAOYSA-N Benzyl alcohol Chemical compound OCC1=CC=CC=C1 WVDDGKGOMKODPV-UHFFFAOYSA-N 0.000 abstract 3
- 229940043232 butyl acetate Drugs 0.000 abstract 3
- 238000006243 chemical reaction Methods 0.000 abstract 3
- FUZZWVXGSFPDMH-UHFFFAOYSA-N hexanoic acid Chemical compound CCCCCC(O)=O FUZZWVXGSFPDMH-UHFFFAOYSA-N 0.000 abstract 3
- AMIMRNSIRUDHCM-UHFFFAOYSA-N Isopropylaldehyde Chemical compound CC(C)C=O AMIMRNSIRUDHCM-UHFFFAOYSA-N 0.000 abstract 2
- 150000001298 alcohols Chemical class 0.000 abstract 2
- 150000001299 aldehydes Chemical class 0.000 abstract 2
- -1 alkaryl alcohols Chemical class 0.000 abstract 2
- 125000003118 aryl group Chemical group 0.000 abstract 2
- HUMNYLRZRPPJDN-UHFFFAOYSA-N benzaldehyde Chemical compound O=CC1=CC=CC=C1 HUMNYLRZRPPJDN-UHFFFAOYSA-N 0.000 abstract 2
- MLUCVPSAIODCQM-NSCUHMNNSA-N crotonaldehyde Chemical compound C\C=C\C=O MLUCVPSAIODCQM-NSCUHMNNSA-N 0.000 abstract 2
- MLUCVPSAIODCQM-UHFFFAOYSA-N crotonaldehyde Natural products CC=CC=O MLUCVPSAIODCQM-UHFFFAOYSA-N 0.000 abstract 2
- 239000007788 liquid Substances 0.000 abstract 2
- BDAGIHXWWSANSR-UHFFFAOYSA-N methanoic acid Natural products OC=O BDAGIHXWWSANSR-UHFFFAOYSA-N 0.000 abstract 2
- 229910000073 phosphorus hydride Inorganic materials 0.000 abstract 2
- HGBOYTHUEUWSSQ-UHFFFAOYSA-N valeric aldehyde Natural products CCCCC=O HGBOYTHUEUWSSQ-UHFFFAOYSA-N 0.000 abstract 2
- QNXQLPUEZYZYFC-UHFFFAOYSA-N (4-nitrophenyl)methyl acetate Chemical compound CC(=O)OCC1=CC=C([N+]([O-])=O)C=C1 QNXQLPUEZYZYFC-UHFFFAOYSA-N 0.000 abstract 1
- OSWFIVFLDKOXQC-UHFFFAOYSA-N 4-(3-methoxyphenyl)aniline Chemical compound COC1=CC=CC(C=2C=CC(N)=CC=2)=C1 OSWFIVFLDKOXQC-UHFFFAOYSA-N 0.000 abstract 1
- BXRFQSNOROATLV-UHFFFAOYSA-N 4-nitrobenzaldehyde Chemical compound [O-][N+](=O)C1=CC=C(C=O)C=C1 BXRFQSNOROATLV-UHFFFAOYSA-N 0.000 abstract 1
- JKTYGPATCNUWKN-UHFFFAOYSA-N 4-nitrobenzyl alcohol Chemical compound OCC1=CC=C([N+]([O-])=O)C=C1 JKTYGPATCNUWKN-UHFFFAOYSA-N 0.000 abstract 1
- LFQSCWFLJHTTHZ-UHFFFAOYSA-N Ethanol Chemical compound CCO LFQSCWFLJHTTHZ-UHFFFAOYSA-N 0.000 abstract 1
- 150000007933 aliphatic carboxylic acids Chemical class 0.000 abstract 1
- 125000001931 aliphatic group Chemical group 0.000 abstract 1
- 125000000217 alkyl group Chemical group 0.000 abstract 1
- 125000005037 alkyl phenyl group Chemical group 0.000 abstract 1
- 150000001450 anions Chemical class 0.000 abstract 1
- RBFQJDQYXXHULB-UHFFFAOYSA-N arsane Chemical group [AsH3] RBFQJDQYXXHULB-UHFFFAOYSA-N 0.000 abstract 1
- 235000019445 benzyl alcohol Nutrition 0.000 abstract 1
- 239000003054 catalyst Substances 0.000 abstract 1
- 235000019253 formic acid Nutrition 0.000 abstract 1
- 229910052741 iridium Inorganic materials 0.000 abstract 1
- 150000002576 ketones Chemical class 0.000 abstract 1
- 239000002184 metal Substances 0.000 abstract 1
- 229910052751 metal Inorganic materials 0.000 abstract 1
- 125000002560 nitrile group Chemical group 0.000 abstract 1
- 125000000449 nitro group Chemical group [O-][N+](*)=O 0.000 abstract 1
- 229910052762 osmium Inorganic materials 0.000 abstract 1
- QNGNSVIICDLXHT-UHFFFAOYSA-N para-ethylbenzaldehyde Natural products CCC1=CC=C(C=O)C=C1 QNGNSVIICDLXHT-UHFFFAOYSA-N 0.000 abstract 1
- 125000001997 phenyl group Chemical group [H]C1=C([H])C([H])=C(*)C([H])=C1[H] 0.000 abstract 1
- 229910052697 platinum Inorganic materials 0.000 abstract 1
- 229910052707 ruthenium Inorganic materials 0.000 abstract 1
- 229920006395 saturated elastomer Polymers 0.000 abstract 1
- 239000002904 solvent Substances 0.000 abstract 1
- 239000000126 substance Substances 0.000 abstract 1
Classifications
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
- C07C29/00—Preparation of compounds having hydroxy or O-metal groups bound to a carbon atom not belonging to a six-membered aromatic ring
- C07C29/132—Preparation of compounds having hydroxy or O-metal groups bound to a carbon atom not belonging to a six-membered aromatic ring by reduction of an oxygen containing functional group
- C07C29/136—Preparation of compounds having hydroxy or O-metal groups bound to a carbon atom not belonging to a six-membered aromatic ring by reduction of an oxygen containing functional group of >C=O containing groups, e.g. —COOH
- C07C29/14—Preparation of compounds having hydroxy or O-metal groups bound to a carbon atom not belonging to a six-membered aromatic ring by reduction of an oxygen containing functional group of >C=O containing groups, e.g. —COOH of a —CHO group
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 |
|---|---|---|---|
| GB3057867 | 1967-07-03 |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| GB1227601A true GB1227601A (enExample) | 1971-04-07 |
Family
ID=10309848
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| GB1227601D Expired GB1227601A (enExample) | 1967-07-03 | 1967-07-03 |
Country Status (1)
| Country | Link |
|---|---|
| GB (1) | GB1227601A (enExample) |
Cited By (2)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| FR2450798A1 (fr) * | 1979-03-08 | 1980-10-03 | Montedison Spa | Procede pour reduire par voie catalytique des composes carbonyles |
| EP0046680A1 (en) * | 1980-08-26 | 1982-03-03 | The Halcon Sd Group, Inc. | Improved catalytic hydrogenation of glycolaldehyde to produce ethylene glycol |
-
1967
- 1967-07-03 GB GB1227601D patent/GB1227601A/en not_active Expired
Cited By (2)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| FR2450798A1 (fr) * | 1979-03-08 | 1980-10-03 | Montedison Spa | Procede pour reduire par voie catalytique des composes carbonyles |
| EP0046680A1 (en) * | 1980-08-26 | 1982-03-03 | The Halcon Sd Group, Inc. | Improved catalytic hydrogenation of glycolaldehyde to produce ethylene glycol |
Similar Documents
| Publication | Publication Date | Title |
|---|---|---|
| NL7100045A (en) | Prodn of transition metal bidentate and - complexes, catalysts for aldehyde/alcohol | |
| Dobscn et al. | Catalytic dehydrogenation of primary and secondary alcohols by Ru (OCOCF3) 2 (CO)(PPh3) 2 | |
| GB1130743A (en) | Organo-iridium complexes | |
| GB1423224A (en) | Production of optically active alcohols | |
| GB1227601A (enExample) | ||
| GB1335531A (en) | Process for producing aldehydes by vapour phase hydroformylation of an olefinically unsaturated organic compound | |
| Blackadder et al. | 554. The kinetics of the decomposition of the addition compounds formed by sodium bisulphite and a series of aldehydes and ketones. Part I | |
| US4239704A (en) | Process for producing acetaldehyde | |
| US3060236A (en) | peocess of producing alpha-beta unsatu- | |
| GB1471481A (en) | Hydroformylation process | |
| GB1462258A (en) | Manufacture of dimethylaminobenzenecarboxylic acid esters | |
| GB1455645A (en) | Production of aliphatic or cycloaliphatic dialdehydes and/or acetals of the same production of 3-sulphopropionic anhydride | |
| GB873263A (en) | Process for preparing condensation products of polyvinyl alcohol and carbonyl compounds | |
| GB1289571A (enExample) | ||
| GB1350822A (en) | Production of alcohols and or aldehydes | |
| GB1232257A (enExample) | ||
| CH551351A (de) | Verfahren zur herstellung von 1,1,2,2-tetrahydroperfluoralkanolen. | |
| GB1337808A (en) | Process for the production of unsaturated aldehydes | |
| GB1141671A (en) | Preparation of -Ï-cyanoalkanoic acids | |
| Humffray et al. | The Hammett σ-value for the formyl group | |
| US3580925A (en) | Imidazole preparation | |
| GB1302374A (enExample) | ||
| ES447636A1 (es) | Metodo de producir 3,5-deterbutil-4-hidroxibenzaldeludo. | |
| GB1421278A (en) | Process for the production of primary amines | |
| NL7507331A (nl) | Werkwijze ter bereiding van 3-acetoxy-2-methylpro- pionaldehyde. |
Legal Events
| Date | Code | Title | Description |
|---|---|---|---|
| PS | Patent sealed | ||
| PLNP | Patent lapsed through nonpayment of renewal fees |