HuagongsheHuagongshe Chemistry Print Report · For research reference only
3-[[5-Methyl-2-(1-methylethyl)cyclohexyl]oxy]-1,2-propanediol → HCID 131723757, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | 3-[[5-Methyl-2-(1-methylethyl)cyclohexyl]oxy]-1,2-propanediol | HCID 5362595 | — |
| Reactant | HCID 131723758 | HCID 131723758 | — |
| Product | HCID 131723757 | HCID 131723757 | 92.38% |
Reaction Steps
The reaction mixture obtained in (1) was mixed with 30 ml of water and 50 ml of heptane to effect separation, the organic layer was washed with saturated brine and dried with anhydrous sodium sulfate, and then the solvent was recovered to obtain an oily substance. By distilling this oily substance under a reduced pressure, partially purified 1-acetoxy-3-l-menthoxypropan-2-ol was obtained at a boiling point of from 111 to 120° C./25 Pa (0.19 mmHg). Composition of this product when analyzed by the gas chromatography was composed of 5.53% by mass of 3-l-menthoxypropane-1,2-diol, 86.04% by mass of 1-acetoxy-3-l-menthoxypropan-2-ol (yield 92.38% based on 1-chloro-3-l-menthoxypropan-2-ol) and 5.13% by mass of 1,2-diacetoxy-3-l-menthoxypropane.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US06515188B2 |
| Source dataset | uspto-grants-2003_02 |
| ORD ID | ord-5d7ce6ee79ad4f2186355ad8a1b58511 |
| Source note | uspto-grants-2003_02 |