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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 253138Generated: October 25, 2026

Sodium Sulfite → 3-(1-(Tert-butyldimethylsilyloxy)cyclobutyl)propane-1,2-diol

https://huagongshe.com/reaction/253138

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSodium SulfiteHCID 24437—
ReactantMethyl morpholine oxideHCID 82029—
Reactant(1-Allylcyclobutoxy)(tert-butyl)dimethylsilaneHCID 66844818—
Reactant2-Methylpropan-2-ol--water (1/1)HCID 71401949—
CatalystOsmium TetroxideHCID 30318—
SolventWaterHCID 962—
Product3-(1-(Tert-butyldimethylsilyloxy)cyclobutyl)propane-1,2-diolHCID 66845148—

Reaction Steps

To a 2 L round bottomed flask was added (1-allylcyclobutoxy) (tert-butyl)dimethylsilane (previous step) and H2O/t-BuOH (1:1, 1 L). NMO (32.68 g, 279 mmol) was added to the mixture. After stirring for 5 min the solution was found to be homogenous. Osmium tetroxide (1.00 g, 3.93 mmol) was added and the reaction was stirred at RT. After 2 h, TLC revealed the reaction to be complete. 500 mL of H2O and sodium sulfite (19.5 g, 155 mmol) were added and the reaction was stirred for another hour. The aqueous solution was extracted with ether (2×1 L). The combined organics were concentrated in vacuo to give 3-(1-(tert-butyldimethylsilyloxy)cyclobutyl)propane-1,2-diol, as a light yellow oil. The oil contained some t-BuOH, but was carried forward without further purification.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07872009B2
Source datasetuspto-grants-2011_01
ORD IDord-aa5b1e4ea92b4414a0676c8fc3e8f0ff
Source noteuspto-grants-2011_01