HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2399984Generated: October 31, 2026
Hydrogen Peroxide → Tert.-Butyl 22-Hydroxydocosanoate
https://huagongshe.com/reaction/2399984
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Hydrogen Peroxide | HCID 784 | — |
| Reactant | Water | HCID 962 | — |
| Reactant | Sodium Hydroxide | HCID 14798 | — |
| Reactant | Docos-21-ynoic Acid. Tert.-Butyl Ester | HCID 86749000 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Solvent | Ethyl Acetate | HCID 8857 | — |
| Product | Tert.-Butyl 22-Hydroxydocosanoate | HCID 19385096 | 54% |
Reaction Steps
A solution of the acetylene (33) (0.4 g, 1.02 mmol) in dry THF (5 ml) at room temperature under nitrogen was treated with borane-dimethyl sulphide complex (1.04 ml of a 2M solution in THF, 2.08 mmol) and the resulting solution stirred for 1 hour, after which time no starting material was present on tlc. The reaction was then treated sequentially with water (2 ml), 2N aqueous sodium hydroxide (1 ml) and 30% hydrogen peroxide (1 ml). The resulting solution was left a further 15 minutes, then ethyl acetate added and the organic layer separated. The aqueous layer was re-extracted with ethyl acetate, the organic layers combined, dried (MgSO4) and evaporated. The crude product obtained in this manner was purified on silica (5 g). Elution with 10% ethyl acetate in petrol gave tert.-butyl 22-hydroxydocosanoate (34) as a white solid (0.23 g, 54%).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|
| Patent number | US05451691 |
|---|
| Source dataset | uspto-grants-1995_09 |
|---|
| ORD ID | ord-1eec539b14ba4a17a555f3b1e237ff30 |
|---|
| Source note | uspto-grants-1995_09 |
|---|