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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1694324Generated: November 3, 2026

Imidazole → Ethyl 5(r)-t-butyldimethylsilyloxyhexanoate

https://huagongshe.com/reaction/1694324

Reaction equation

Participants

RoleNameHCIDCharge
ReactantImidazoleHCID 795—
Reactanttert-Butyldimethylsilyl chlorideHCID 28928—
ReactantEthyl 5(R)-hydroxyhexanoateHCID 11073717—
SolventDimethylformamideHCID 6228—
ProductEthyl 5(r)-t-butyldimethylsilyloxyhexanoateHCID 1051649188%

Reaction Steps

A solution of ethyl 5(R)-hydroxyhexanoate 3 (1.80 g, 11.24 mmol), imidazole (2.3 g, 33.8 mmol), and t-butyldimethylsilyl chloride (2.54 g, 16.85 mmol) in 30 mL of DMF was stirred at 23° C. overnight (19 h). The solvent (DMF) was then removed in vacuo and aqueous saturated sodium bicarbonate (100 mL) was added followed by ethyl acetate (100 mL). The layers were separated and the aqueous layer was re-extracted with 100 mL of EtOAc. The combined organic layers were washed with water, brine, and dried over anhydrous sodium sulfate. Flash column chromatographic purification on 30 g of silica gel yielded 2.71 g (88%) of TBDMS-ether 4 (G.C. purity of 99+A %); 1H NMR (CDCl3): 0.04 (s, 6H), 0.91 (s, 9H), 1.18 (d, J=6 Hz, 3H), 1.25 (t, J=7.2 Hz, 3H), 1.42 (m, 2H), 1.65 (m, 2H), 2.39 (t, J=7.5 Hz, 2H), 3.79 (m, J=6 Hz, 1H), 4.12 (q, J=7.2 Hz, 2H).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08158676B2
Source datasetuspto-grants-2012_04
ORD IDord-2acd8b13dfb64c339b9debb45f54ee42
Source noteuspto-grants-2012_04