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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 741668Generated: October 30, 2026

Ozone → 3-(Tertbutyldiphenylsilyloxymethylene)-pentane-1,5-diol

https://huagongshe.com/reaction/741668

Reaction equation

Participants

RoleNameHCIDCharge
ReactantOzoneHCID 24823—
ReactantSodium borohydrideHCID 4311764—
Reactant3-(Tert-butyldiphenylsilyloxymethylene)-1,5-pentanediolHCID 18790449—
SolventMethanolHCID 887—
Product3-(Tertbutyldiphenylsilyloxymethylene)-pentane-1,5-diolHCID 131719533—

Reaction Steps

Ozone was bubbled through a -78° C. dry methanol (500 mL) solution of 3-(tert-butyldiphenylsilyloxymethylene)-1,5-pentanediol (17 g, 47 mmol) until a blue tint persisted (30 minutes). The reaction was purged with nitrogen (20 min.) and NaBH4 (17.6 g, 47 mmol) was added. The cold bath was removed and the reaction brought to room temperature. The reaction was concentrated in vacuo and the residue partitioned between ether and brine. The ether layer was concentrated and the residue eluted over a silica plug with 0-50% ethyl acetate/hexanes. The minor component was pooled and concentrated to yield the diol , 3-(tertbutyldiphenylsilyloxymethylene)-pentane-1,5-diol, 3.8 g (22%) of the desired diol as a colorless oil. Overall the yield for the three steps is 17%. MS.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05552396
Source datasetuspto-grants-1996_09
ORD IDord-bc3039f4aa6f45af8f7656f45664ab30
Source noteuspto-grants-1996_09