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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 514806Generated: October 31, 2026

Sulfuric Acid → HCID 89141974, compound

https://huagongshe.com/reaction/514806

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSulfuric AcidHCID 1118—
ReactantAmmonium ChlorideHCID 25517—
Reactant3-Bromo-2-methyl-1-propeneHCID 357785—
Reactanttert-Butyl 4-oxopiperidine-1-carboxylateHCID 735900—
CatalystZincHCID 23994—
SolventWaterHCID 962—
SolventTetrahydrofuranHCID 8028—
SolventEthylacetate heptaneHCID 21899848—
ProductHCID 89141974HCID 8914197496.2%

Reaction Conditions

Temperature10 °C

Reaction Steps

t-butyl-4-oxopiperidine-1-carboxylate (10 g, 0.05 mol) was dissolved in 3-bromo-2-methylprop-1-ene (16.9 g, 0.126 mol), THF (100 mL) and saturated ammonium chloride solution (500 mL). The reaction was cooled to 10° C. and zinc dust (6.6 g, 0.01 mol) was added portionwise. After addition, the reaction mixture was stirred overnight, when TLC (heptane/EtOAc 7:1) indicated that the reaction was complete. The reaction mixture was then diluted with water and acidified with 10% H2SO4 to pH 6. The reaction mixture was extracted with ethyl acetate (3×50 mL). The organic layers were combined and washed with saturated solution of NaHCO3, brine and evaporated to give tert-butyl 4-hydroxy-4-(2-methylallyl)piperidine-1-carboxylate (12.28 g). 1H NMR (CHLOROFORM-d) δ: 4.94-5.04 (m, 1H), 4.80 (s, 1H), 3.85 (dt, J=13.0, 3.4 Hz, 2H), 3.08-3.26 (m, 2H), 2.21 (s, 2H), 1.86 (s, 3H), 1.52-1.60 (m, 4H), 1.43-1.50 (m, 9H).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09108921B2
Source datasetuspto-grants-2015_08
ORD IDord-5faf6a5027d34c48809f8c438d9ed99e
Source noteuspto-grants-2015_08