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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1939261Generated: October 29, 2026

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

https://huagongshe.com/reaction/1939261

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 (17.6g, 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 numberUS05696108
Source datasetuspto-grants-1997_12
ORD IDord-11daa2c94b244b52a50d2652627413eb
Source noteuspto-grants-1997_12