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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 723457Generated: October 25, 2026

Tetrahydrofuran → tert-Butyl 4-azido-3-hydroxypiperidine-1-carboxylate

https://huagongshe.com/reaction/723457

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTetrahydrofuranHCID 8028—
ReactantAmmonium ChlorideHCID 25517—
ReactantLithium tri-s-butylborohydrideHCID 3611392—
Reactant(+/-)-Tert-butyl 4-azido-3-oxopiperidine-1-carboxylateHCID 21874153—
SolventWaterHCID 962—
Producttert-Butyl 4-azido-3-hydroxypiperidine-1-carboxylateHCID 21874176—

Reaction Conditions

Temperature-78 °C

Reaction Steps

To a solution of Compound 201A prepared above in dry THF (2 mL) cooled at −78° C. was added L-Selectride (1.0 M in THF, 0.98 mL, 0.98 mmol). The mixture was stirred at −78° C. for 2.0 hrs. Saturated NH4Cl (2 mL) was added and the reaction mixture was allowed to warm to room temperature. The mixture was diluted with water and extracted with EtOAc (3×). The combined organic layers were washed once with brine and dried over anhydrous Na2SO4. Concentration in vacuo followed by flash chromatography (hexane-EtOAc 4:1) on silica gel gave 44 mg of Compound 201B as an oil. 1H-NMR (400 MHz, CDCl3): 3.84 (m, 1H), 3.69 (m, 1H), 3.58 (m, 2H), 3.40 (m, 1H), 3.30 (m, 1H), 1.96 (m, 1H), 1.73 (m, 1H), 1.46 (s, 9H).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07141571B2
Source datasetuspto-grants-2006_11
ORD IDord-d058b9f470174969b4623e7ee84d6d73
Source noteuspto-grants-2006_11