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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1476744Generated: October 30, 2026

Acetic Acid → HCID 86707207, compound

https://huagongshe.com/reaction/1476744

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAcetic AcidHCID 176—
ReactantSodium triacetoxyborohydrideHCID 5049666—
Reactant2-(4-Fluorophenoxy)acetaldehydeHCID 11051869—
ReactantHCID 86707208HCID 86707208—
Solvent1,2-DichloroethaneHCID 11—
ProductHCID 86707207HCID 8670720770.4%

Reaction Steps

Stir a mixture of methyl 4-[(1S)-1-[[(2R)-piperidine-2-carbonyl]amino]ethyl]benzoate hydrochloride (650 mg, 1.99 mmol) and 2-(4-fluorophenoxy)acetaldehyde (337 mg, 2.19 mmol) in DCE (9.9 mL) at room temperature for 30 min. Add acetic acid (0.113 mL, 1.99 mmol) and sodium triacetoxyborohydride (590 mg, 2.78 mmol) and stir at room temperature for three days. Quench the reaction with saturated aqueous NaHCO3 (25 mL) and extract the aqueous layer with EtOAc (2×25 mL). Wash the combined organic layers with saturated aqueous NaCl (25 mL), then dry the organic phase over MgSO4, filter, and concentrate under reduced pressure. Subject the resulting oil to flash chromatography on silica gel, eluting with a gradient of 0% to 100% EtOAc/hexanes. Concentrate the fractions containing the desired product under reduced pressure to provide the title compound as a white solid (600 mg, 70% yield). Mass spectrum (m/z) 429 (M+H)+, 451 (M+Na)+.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09402838B2
Source datasetuspto-grants-2016_08
ORD IDord-b3b1e6ea09cd47ea912360d7a83b5a77
Source noteuspto-grants-2016_08