Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 368518Generated: October 31, 2026

Potassium Carbonate → Tert-butyl 4-(hydroxymethyl)piperidine-1-carboxylate

https://huagongshe.com/reaction/368518

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPotassium CarbonateHCID 11430—
Reactant1-(tert-Butoxycarbonyl)-4-piperidinecarboxylic acidHCID 392871—
ReactantBorane;tetrahydrofuranHCID 2723981—
SolventWaterHCID 962—
ProductTert-butyl 4-(hydroxymethyl)piperidine-1-carboxylateHCID 276408184.5%

Reaction Conditions

Temperature0 °C

Reaction Steps

Borane-tetrahydrofuran (1 M, 25 mL, 25 mmol) was added slowly to N-tert-butoxycarbonylisonipecotic acid (5.73 g, 25 mmol), as prepared in the preceding step, in tetrahydrofyiran (50 mL) at 0° C. (ice-bath) over 30 min. The mixture was stirred at 0° C. overnight and then warmed up to room temperature for 6 h. Water (10 mL) was added slowly and then K2CO3 (5 g in 50 mL water) was added. The mixture was extracted with ethyl acetate (3×50 mL). The organic phase was washed sequentially with saturated NaHCO3 (2×50 mL) and brine (2×50 mL), and dried over Na2SO4. The solvent was removed in vacuo, and the residue was purified by flash column chromatography (1:1 hexane/ethyl acetate) to give the title compound as white crystals (4.55 g, 84%). 1H-NMR (300 MHz, CDCl3) δ 1.13 (m, 2 H), 1.42 (s, 9 H), 1.67 (m, 4 H), 2.67 (t, 2 H, J=12.5 Hz), 3.46 (d, 2 H, J=3.0 Hz), and 4.09 (d, 2 H, J=3.6 Hz).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06133315
Source datasetuspto-grants-2000_10
ORD IDord-c82707bb1e1347ecb3dd1b2c9db6f964
Source noteuspto-grants-2000_10