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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 54022Generated: October 29, 2026

Ozone → HCID 28562535, compound

https://huagongshe.com/reaction/54022

Reaction equation

Participants

RoleNameHCIDCharge
ReactantOzoneHCID 24823—
ReactantSodium borohydrideHCID 4311764—
Reactant[2-(Allyloxy)phenyl]methanolHCID 11137475—
SolventMethanolHCID 887—
ProductHCID 28562535HCID 2856253567%

Reaction Steps

Ozone was bubbled through a -78° C. dry methanol solution of 2-(allyloxy)benzyl alcohol (LaChapelle et al Tetrahedron, 44(16), 5033-5044 (1988)) (7.0 g, 43 mmol) for 13 minutes, checking the reaction TLC profile every 2 minutes for complete disappearance of the starting olefin (Rf=0.8, 75% EtOAc/hexane). The reaction mixture was purged with nitrogen, NaBH4 (9.7 g, 0.25 mol) was added and the reaction temperature brought to 0° C. After 30 minutes, the reaction was warmed to room temperature, concentrated, diluted with ether, washed with water, brine, dried and concentrated to a residue. The residue was eluted through a pad of silica with EtOAc/hexanes (gradient elution 25%-75% EtOAC). Evaporation of the eluting solvent gave the diol, 2-(2'-hydroxyethoxy)-benzyl alcohol, (4.8 g, 67%) as an oil. MS: MW=168; observed 168, FD, CHCl3).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05621098
Source datasetuspto-grants-1997_04
ORD IDord-871d451aa63f438e937e52c59106cc89
Source noteuspto-grants-1997_04