BE346225A - - Google Patents
Info
- Publication number
- BE346225A BE346225A BE346225DA BE346225A BE 346225 A BE346225 A BE 346225A BE 346225D A BE346225D A BE 346225DA BE 346225 A BE346225 A BE 346225A
- Authority
- BE
- Belgium
- Prior art keywords
- ethereal
- thymol
- hydrogenation
- products
- isomers
- Prior art date
Links
- MGSRCZKZVOBKFT-UHFFFAOYSA-N thymol Chemical compound CC(C)C1=CC=C(C)C=C1O MGSRCZKZVOBKFT-UHFFFAOYSA-N 0.000 claims description 8
- 239000007859 condensation product Substances 0.000 claims description 5
- UFHFLCQGNIYNRP-UHFFFAOYSA-N Hydrogen Chemical compound [H][H] UFHFLCQGNIYNRP-UHFFFAOYSA-N 0.000 claims description 4
- 239000005844 Thymol Substances 0.000 claims description 4
- 238000005984 hydrogenation reaction Methods 0.000 claims description 4
- 229960000790 thymol Drugs 0.000 claims description 4
- 125000004435 hydrogen atom Chemical group [H]* 0.000 claims description 3
- 150000002576 ketones Chemical class 0.000 claims description 3
- 150000002989 phenols Chemical class 0.000 claims description 3
- 239000000047 product Substances 0.000 claims description 3
- 239000003054 catalyst Substances 0.000 claims description 2
- 238000000034 method Methods 0.000 claims 1
- 238000002360 preparation method Methods 0.000 claims 1
- CSCPPACGZOOCGX-UHFFFAOYSA-N Acetone Chemical compound CC(C)=O CSCPPACGZOOCGX-UHFFFAOYSA-N 0.000 description 6
- IWDCLRJOBJJRNH-UHFFFAOYSA-N p-cresol Chemical compound CC1=CC=C(O)C=C1 IWDCLRJOBJJRNH-UHFFFAOYSA-N 0.000 description 4
- 229910052739 hydrogen Inorganic materials 0.000 description 3
- 239000001257 hydrogen Substances 0.000 description 3
- RLSSMJSEOOYNOY-UHFFFAOYSA-N m-cresol Chemical compound CC1=CC=CC(O)=C1 RLSSMJSEOOYNOY-UHFFFAOYSA-N 0.000 description 2
- 239000000203 mixture Substances 0.000 description 2
- CRBJBYGJVIBWIY-UHFFFAOYSA-N 2-isopropylphenol Chemical compound CC(C)C1=CC=CC=C1O CRBJBYGJVIBWIY-UHFFFAOYSA-N 0.000 description 1
- 125000004429 atom Chemical group 0.000 description 1
- 230000005494 condensation Effects 0.000 description 1
- 238000009833 condensation Methods 0.000 description 1
- 238000004519 manufacturing process Methods 0.000 description 1
Classifications
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
- C07C35/00—Compounds having at least one hydroxy or O-metal group bound to a carbon atom of a ring other than a six-membered aromatic ring
- C07C35/02—Compounds having at least one hydroxy or O-metal group bound to a carbon atom of a ring other than a six-membered aromatic ring monocyclic
- C07C35/08—Compounds having at least one hydroxy or O-metal group bound to a carbon atom of a ring other than a six-membered aromatic ring monocyclic containing a six-membered rings
- C07C35/12—Menthol
Landscapes
- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Low-Molecular Organic Synthesis Reactions Using Catalysts (AREA)
- Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)
Publications (1)
Publication Number | Publication Date |
---|---|
BE346225A true BE346225A (enrdf_load_stackoverflow) |
Family
ID=22118
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
BE346225D BE346225A (enrdf_load_stackoverflow) |
Country Status (1)
Country | Link |
---|---|
BE (1) | BE346225A (enrdf_load_stackoverflow) |
-
0
- BE BE346225D patent/BE346225A/fr unknown
Similar Documents
Publication | Publication Date | Title |
---|---|---|
CA1258873A (en) | Process for the production of 2-ethyl-hexanol | |
CROSSLEY et al. | Studies on the Leuckart reaction | |
Milas et al. | Organic peroxides. XIX. α-Hydroperoxyethers and related peroxides | |
Pratt et al. | Disproportionative Condensations. I. Modified Guerbet Reactions | |
BE346225A (enrdf_load_stackoverflow) | ||
US2108133A (en) | Process for producing high molecular alcohols from the corresponding ketones | |
Dawson et al. | Synthesis of compounds structurally related to poison ivy urushiol. 3. 3-n-Pentadecylcatechol and 3-n-alkylcatechols of varying side-chain length | |
US2315046A (en) | Production of ketones | |
US3184432A (en) | Process for the production of cyclododecane derivatives | |
US2553470A (en) | Production of alkenyl phenols | |
Suter et al. | α, β-Dialkylphenethylamines. Alkylation of Phenylacetone | |
US2761877A (en) | Production of phenols and carbonyl compounds | |
US2537647A (en) | Rearrangement of terpenyl aryl ethers | |
Elslager et al. | Synthesis and Biological Properties of Aminoalkylhydrazines. A Unique Nitrogen-nitrogen Scission of 1-(2-diethylaminoethyl)-2-(1-phenyl-2-propyl) hydrazine | |
Roberti et al. | Preparation of 3, 4-Dimethoxyphenyl-and 4-Hydroxy-3-methoxyphenylalkylcarbinols | |
US3624136A (en) | Method of preparing catechol diacetates | |
US2471454A (en) | Process for catalytic condensation of phenols with monocyclic dihydroterpenes | |
CA1200254A (fr) | Procede de preparation d'alcools orthohydroxybenzyliques | |
US2737527A (en) | Production of phenols and carbonyl compounds | |
US2572563A (en) | Aromatic compositions and process of treating lactone material to prepare them | |
BE352651A (enrdf_load_stackoverflow) | ||
Bader | Cyclopentenylphenols | |
Nightingale et al. | The Action of Nitrous Acid on 2-Phenylcyclohexylamine | |
US4133835A (en) | Process for bi-organic peroxides | |
EP0967194A1 (en) | Preparation of di-tert-peroxides |