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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 392543Generated: October 26, 2026

Water → (S)-Glycidoxy-t-butyldimethylsilane

https://huagongshe.com/reaction/392543

Reaction equation

Participants

RoleNameHCIDCharge
ReactantWaterHCID 962—
Reactant(-)-Benzyl (R)-glycidyl etherHCID 159746—
Reactanttert-Butyldimethylsilyl glycidyl etherHCID 3605359—
CatalystAcetic AcidHCID 176—
SolventTetrahydrofuranHCID 8028—
Product(S)-Glycidoxy-t-butyldimethylsilaneHCID 1095430748.3%

Reaction Steps

Using the (R,R)-(salen)Co(II) precatalyst of 1 (91 mg, 0.15 mmol, 0.005equiv), (+/−)-(tert-butyldimethylsilyl) glycidyl ether (5.64 g, 30.0 mmol), AcOH (32 mL, 0.6 mmol, 0.02 equiv), 0.3 mL THF, and H2O (297 mL, 16.5 mmol, 0.55 equiv) and a procedure analogous to the one outlined for 5b, (S)-(tert-butyldimethylsilyl) glycidyl ether 5c (2.72 g, 14.5 mmol, 48%) was obtained as a clear oil by vacuum distillation of the reaction mixture (30° C., 0.5 Torr). The product was determined to be present in >99% ee by derivatization through ring opening with 2-napthalenethiol in methanol using 1 equiv TEA at 0° C. and direct analysis of the 2-napthylsulfide thus obtained (Chiralcel OD, 99.25:0.75 hexanes:EtOH, 1 mL/min, 230 nm).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06800766B2
Source datasetuspto-grants-2004_10
ORD IDord-9beb00fcd253446d865520dc1494ea0b
Source noteuspto-grants-2004_10