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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2213038Generated: October 31, 2026

Water → HCID 53446371, compound

https://huagongshe.com/reaction/2213038

Reaction equation

Participants

RoleNameHCIDCharge
ReactantWaterHCID 962—
ReactantHomoallyl bromideHCID 21241—
ReactantLithium HexamethyldisilazideHCID 2733832—
Reactant4-Benzyl 1-tert-butyl piperidine-1,4-dicarboxylateHCID 22255913—
SolventTetrahydrofuranHCID 8028—
ProductHCID 53446371HCID 5344637137%

Reaction Conditions

Temperature-78 °C

Reaction Steps

Lithium hexamethyldisilazide (1M in tetrahydrofuran, 15.7 mL, 15.7 mmol) was added dropwise to a stirred, cooled (−78° C.) solution of 1-(1,1-dimethylethyl) 4-phenylmethyl 1,4-piperidinedicarboxylate (2.50 g, 7.83 mmol) in tetrahydrofuran (50 mL) and the mixture was stirred at −78° C. for 2 hours. 4-Bromo-1-butene (1.99 mL, 19.6 mmol) was added dropwise and the mixture was stirred at −78° C. for 1 hour, then at room temperature for 2 hours. Water (100 mL) was added and the mixture was extracted with ethyl acetate (2×100 mL). The combined organic fractions were dried (MgSO4) and the solvent was evaporated under reduced pressure. The residue was purified by flash column chromatography on silica gel, eluting with isohexane/EtOAc (90:10) to give the title compound (1.07 g, 37%). 1H NMR (400 MHz CDCl3) δ 7.4–7.3 (5H, m), 5.75–5.6 (1H, m), 5.15 (2H, s), 4.93 (1H, br d, J 7 Hz), 4.90 (1H, br s), 3.95–3.75 (2H, m), 2.93–2.78 (2H, m), 2.13 (2H, br d, J 10 Hz), 1.95–1.85 (2H, m), 1.65–1.55 (2H, m), 1.44 (9H, s), and 1.43–1.30 (2H, m).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07105507B2
Source datasetuspto-grants-2006_09
ORD IDord-8cf16cbefa77473bae626586e5ed824c
Source noteuspto-grants-2006_09