HuagongsheHuagongshe Chemistry Print Report · For research reference only
Water → Ethyl 11-hydroxy-3,7,11-trimethyldodeca-2,4-dienoate
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Water | HCID 962 | — |
| Reactant | Tetrahydrofuran | HCID 8028 | — |
| Reactant | Sodium borohydride | HCID 4311764 | — |
| Reactant | trans Ethyl 3,7,11-trimethyldodeca-2,4,10-trienoate | HCID 86733725 | — |
| Solvent | Sodium Hydroxide | HCID 14798 | — |
| Product | Ethyl 11-hydroxy-3,7,11-trimethyldodeca-2,4-dienoate | HCID 54480983 | — |
Reaction Steps
To a mixture of 1.9 g. of mercuric acetate, 6 ml. of water and 20 ml. of tetrahydrofuran is added 1.49 g. of trans ethyl 3,7,11-trimethyldodeca-2,4,10-trienoate slowly. After addition is complete, the reaction mixture is stirred for about 20 minutes. The mixture is cooled to about 0° and 6 ml. of aqueous sodium hydroxide (3 molar) is added followed by 0.49 g. of sodium borohydride in aqueous sodium hydroxide (about 3 molar). The mixture is stirred for about 30 minutes. The mixture is then decanted, concentrated, diluted with water and then extracted with ether. The ethereal extract is washed with water, dried over magnesium sulfate and the product chromatographed on silica gives ethyl 11-hydroxy-3,7,11-trimethyldodeca-2,4-dienoate (trans).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US03970704 |
| Source dataset | uspto-grants-1976_07 |
| ORD ID | ord-f2d28bfb571b43f386da1dfeae8c026b |
| Source note | uspto-grants-1976_07 |