HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1098136Generated: October 26, 2026
Imidazole → Methyl 5-(tert-butyl-dimethylsilyl)oxypentanoate
https://huagongshe.com/reaction/1098136
Participants
| Role | Name | HCID | Charge |
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| Reactant | Imidazole | HCID 795 | — |
| Reactant | tert-Butyldimethylsilyl chloride | HCID 28928 | — |
| Reactant | Pentanoic acid, 5-hydroxy-, methyl ester | HCID 3014818 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | Methyl 5-(tert-butyl-dimethylsilyl)oxypentanoate | HCID 11139432 | 52% |
Reaction Steps
A solution of tert-butylchlorodimethylsilane (27.1 g, 179.79 mmol) in DCM (50 mL) was added dropwise to a stirred solution of methyl 5-hydroxypentanoate (CAS no. 14273-92-8, Huckstep, M.; Taylor, R. J. K.; Caton, M. P. L. Synthesis 1982, 10, 881) (19.8 g, 149.82 mmol) and 1H-imidazole (15.30 g, 224.73 mmol) in DCM (200 mL) at 5° C., over a period of 10 minutes under nitrogen. The resulting suspension was stirred at ambient temperature for 6 hours. The reaction mixture was diluted with DCM (250 mL), and washed sequentially with water (2×200 mL) and saturated brine (200 mL). The organic layer was dried (MgSO4) and evaporated. The residue was purified by flash silica chromatography, eluting with 10 to 50% ethyl acetate in isohexane to afford the product (19.3 g, 52%).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08143263B2 |
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| Source dataset | uspto-grants-2012_03 |
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| ORD ID | ord-c3e8a6411ea7432b85eed9fffce967b1 |
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| Source note | uspto-grants-2012_03 |
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