Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1640529Generated: October 26, 2026

Hydrochloric Acid → Rac-5-[4-(tert-butyl-dimethyl-silanyloxy)-butyl]-3-(2,3-dihydro-benzo[1,4]dioxin-6-yl)-oxazolidin-2-one

https://huagongshe.com/reaction/1640529

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydrochloric AcidHCID 313—
ReactantTetrahydrofuranHCID 8028—
ReactantRac-tert-butyl-dimethyl-(4-oxiranyl-butoxy)-silaneHCID 13570755—
Reactant(2,3-Dihydro-benzo[1,4]dioxin-6-yl)-carbamic acid benzyl esterHCID 66736198—
ReactantHCID 178506942HCID 178506942—
SolventDimethylformamideHCID 6228—
ProductRac-5-[4-(tert-butyl-dimethyl-silanyloxy)-butyl]-3-(2,3-dihydro-benzo[1,4]dioxin-6-yl)-oxazolidin-2-oneHCID 6673736882.1%

Reaction Steps

A solution of (2,3-dihydro-benzo[1,4]dioxin-6-yl)-carbamic acid benzyl ester (0.75 g, 2.6 mmol) and rac-tert-butyl-dimethyl-(4-oxiranyl-butoxy)-silane (prepared according to Angew. Chem. (2007), 46, 5896; 0.91 g, 1.5 eq.) in DMF (8 mL) at 0° C. was treated with a 2.2M solution of t-BuOLi in THF (3.6 mL, 3 eq.). The mixture was stirred at rt for 22 h. HCl 1M (5.3 mL) was added and the mixture partitioned between EA and water. The org. phase was washed with water and brine, dried over MgSO4 and concentrated. The product was purified by FC (Hex/EA 1:1, 1:2) to give the title intermediate as a yellowish oil (0.87 g, 81% yield).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08114867B2
Source datasetuspto-grants-2012_02
ORD IDord-d3852a30700c46a3a26e2e4a7ca013b5
Source noteuspto-grants-2012_02