HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1037721Generated: October 30, 2026
Imidazole → Ethyl 5(r)-t-butyldimethylsilyloxyhexanoate
https://huagongshe.com/reaction/1037721
Participants
| Role | Name | HCID | Charge |
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| Reactant | Imidazole | HCID 795 | — |
| Reactant | tert-Butyldimethylsilyl chloride | HCID 28928 | — |
| Reactant | Ethyl 5(R)-hydroxyhexanoate | HCID 11073717 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Product | Ethyl 5(r)-t-butyldimethylsilyloxyhexanoate | HCID 10516491 | 88% |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08546603B2 |
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| Source dataset | uspto-grants-2013_10 |
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| ORD ID | ord-65c1d404d589410cb87c13c4a5d1c802 |
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| Source note | uspto-grants-2013_10 |
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