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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1455931Generated: November 4, 2026

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

https://huagongshe.com/reaction/1455931

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, 3.8g (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 numberUS05843935
Source datasetuspto-grants-1998_12
ORD IDord-eed0a14daa2a40bc8e970bc8d3171622
Source noteuspto-grants-1998_12