Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Water | HCID 962 | — |
| Reactant | 1-(Hydroxymethyl)-cyclohexanecarboxaldehyde | HCID 13106397 | — |
| Reactant | Methanol--water (1/1) | HCID 22242641 | — |
| Solvent | Methanol | HCID 887 | — |
| Product | Cyclohexanemethanol | HCID 7507 | — |
| Product | Cyclohexanedimethanol | HCID 250594 | — |
| Product | 1-(Hydroxymethyl)-cyclohexanecarboxaldehyde | HCID 13106397 | — |
Reaction Steps
Using the method described in Example 1(b), 1.4 parts per hour of a 60 percent strength by weight solution of 1-hydroxymethyl-hexahydro-benzaldehyde in a 1:1 water-methanol mixture are hydrogenated, over the catalyst prepared as described in Example 1(a), at 130° C. and 30 bar, with a throughput of 0.42 part of 1-hydroxymethyl-hexahydrobenzaldehyde per liter of catalyst per hour. The conversion is 99 percent. The hydrogenated material is fractionated through a packed column. After first runnings of water, methanol and small amounts of hexahydrobenzyl alcohol and 1-hydroxymethyl-hexahydrobenzaldehyde, 1,1-di-hydroxymethylcyclohexane, of boiling point 120°-122° C./3 mbar (melting point 90°-92° C.), is obtained in an amount corresponding to 0.8314 part per hour. This is equivalent to a yield of 97.6% of theory, based on starting material.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US04393251 |
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| Source dataset | uspto-grants-1983_07 |
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| ORD ID | ord-24cbc4edd5a0445ebacedb27de85b7f9 |
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| Source note | uspto-grants-1983_07 |
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