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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2035637Generated: October 29, 2026

Hydrochloric Acid → tert-Butyl 3,3-difluoro-4-hydroxypiperidine-1-carboxylate

https://huagongshe.com/reaction/2035637

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydrochloric AcidHCID 313—
ReactantSodium BicarbonateHCID 516892—
ReactantSodium borohydrideHCID 4311764—
Reactanttert-Butyl 3,3-difluoro-4,4-dihydroxypiperidine-1-carboxylateHCID 57415845—
SolventEthanolHCID 702—
Producttert-Butyl 3,3-difluoro-4-hydroxypiperidine-1-carboxylateHCID 5693210648%

Reaction Steps

tert-Butyl 3,3-difluoro-4,4-dihydroxypiperidine-1-carboxylate (3.10 g, 12.2 mmol) was dissolved in 95% EtOH (50 mL) and the solution was treated with sodium borohydride (2.32 g, 61.2 mmol) and stirred at ambient temperature for 3 hours. The reaction was treated dropwise with 3N HCl until vigorous gas evolution ceased, then stirred at ambient temperature for 20 minutes (pH of the mixture was 3-4 at this point). The reaction was neutralized with saturated NaHCO3 and concentrated in vacuo. The residue was dissolved in ethyl acetate and water and the layers were separated. The aqueous layer was washed with ethyl acetate and the combined organic layers were washed with saturated NaCl, dried over Na2SO4 and concentrated in vacuo to provide the desired product as a white solid (1.39 g).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08575145B2
Source datasetuspto-grants-2013_11
ORD IDord-00671a0412d44b4c954a252db5d50524
Source noteuspto-grants-2013_11