Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2399984Generated: October 31, 2026

Hydrogen Peroxide → Tert.-Butyl 22-Hydroxydocosanoate

https://huagongshe.com/reaction/2399984

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydrogen PeroxideHCID 784—
ReactantWaterHCID 962—
ReactantSodium HydroxideHCID 14798—
ReactantDocos-21-ynoic Acid. Tert.-Butyl EsterHCID 86749000—
SolventTetrahydrofuranHCID 8028—
SolventEthyl AcetateHCID 8857—
ProductTert.-Butyl 22-HydroxydocosanoateHCID 1938509654%

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

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05451691
Source datasetuspto-grants-1995_09
ORD IDord-1eec539b14ba4a17a555f3b1e237ff30
Source noteuspto-grants-1995_09