HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1659825Generated: November 2, 2026
Potassium Hydroxide → 1-Dodecanol, 3,7,11-trimethyl-, (R*,R*)-
https://huagongshe.com/reaction/1659825
Participants
| Role | Name | HCID | Charge |
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| Reactant | Potassium Hydroxide | HCID 14797 | — |
| Reactant | Potassium Acetate | HCID 517044 | — |
| Reactant | HCID 13191849 | HCID 13191849 | — |
| Solvent | Chloroform | HCID 6212 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Product | 1-Dodecanol, 3,7,11-trimethyl-, (R*,R*)- | HCID 159064 | 94% |
Reaction Steps
For the verification of the optical purity the compound obtained is hydrogenated on pre-hydrogenated platinum dioxide to (3R,7R)-1-chloro-3,7,11-trimethyldodecane; boiling point at 0.07 mm; 90°; αD =-1.2° (4.08% in CHCl3), which is converted by heating with dry potassium acetate in dimethylformamide (4 hours at 170°). This ester is purified by adsorption on silicagel (elution agent: n-hexane/ether 4+1), then further reacted to (3R,7R)-3,7,11-trimethyl-1-dodecanol by stirring with 4-N aqurous caustic potash (30 min. at room temperature). The mixture is extracted, washed neutral, dried, concentrated, distilled in the bulb-tube (115°, 0.20 Torr) and there is obtained (3R,7R)-3,7,11-trimethyl-1-dodecanol in 94% yield (based on (3R,7R)-1-chloro-3,7,11-trimethyldodecane employed). The product has an optical rotation value of [α]D20 =+3.7° (4.14% in n-octane) and is accordingly identical with authentic material.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US04305876 |
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| Source dataset | uspto-grants-1981_12 |
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| ORD ID | ord-5f90aaec506c4d6ab56ea40175b40aae |
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| Source note | uspto-grants-1981_12 |
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