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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1714403Generated: October 27, 2026

Sodium Hydroxide → Trans 4-(2-Chloro-4-fluoro-phenoxy)-3-hydroxy-piperidine-1-carboxylic acid tert-butyl ester

https://huagongshe.com/reaction/1714403

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSodium HydroxideHCID 14798—
ReactantAmmonium ChlorideHCID 25517—
Reactant2-Chloro-4-fluorophenolHCID 74814—
Reactanttert-butyl (1S,6R)-7-oxa-3-azabicyclo[4.1.0]heptane-3-carboxylateHCID 55273474—
Solvent1,4-DioxaneHCID 31275—
SolventEthylacetate heptaneHCID 21899848—
ProductTrans 4-(2-Chloro-4-fluoro-phenoxy)-3-hydroxy-piperidine-1-carboxylic acid tert-butyl esterHCID 68506255—

Reaction Steps

Rac-cis-7-Oxa-3-aza-bicyclo[4.1.0]heptane-3-carboxylic acid tert-butyl ester (1 g, 5 mmol) was solvated in dioxane (5 mL), 2-Chloro-4-Fluorophenol was added (1.471 g, 10 mmol) and sodium hydroxide (0.401 g, 10 mmol). After 20 hours refluxing, the mixture was cooled, ammonium chloride was added and the mixture extracted three times with ethyl acetate. The combined organic phases were dried with magnesium sulfate and concentrated under vacuum. After a flash chromatography with heptane/ethyl acetate 1:1 to 1:2 heptane/ethyl acetate a solid the title compound was obtained as solid (0.778 g, 45% yield). MS (m/e): 404.5 (M+AcO−).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07795437B2
Source datasetuspto-grants-2010_09
ORD IDord-0f043f77be3f4268a079654f59e3fdfa
Source noteuspto-grants-2010_09