Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 491593Generated: October 31, 2026

Acetic Acid → HCID 17756290, compound

https://huagongshe.com/reaction/491593

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAcetic AcidHCID 176—
ReactantFormaldehydeHCID 712—
ReactantSodium cyanoborohydrideHCID 5003444—
Reactant(2S)-2-[(2-Chloro-5-nitrophenoxy)methyl]pyrrolidineHCID 17755967—
SolventAcetonitrileHCID 6342—
ProductHCID 17756290HCID 17756290—

Reaction Steps

To (S)-2-(2-chloro-5-nitro-phenoxymethyl)-pyrrolidine (4.82 g, 18.77 mmol) in 167 mL CH3CN at RT was added 37% aqueous formaldehyde (7.58 mL) then NaCNBH3 (1.887 g, 30.03 mmol). The reaction was stirred for 1 h, as the reaction pH was adjusted every 10 min to about 7 by adding small amounts of HOAc. The reaction was concentrated to small aqueous volume and dissolved into 2 N NaOH (aq) and Et2O. The layers were separated, and the organic layer was washed twice with 2 N NaOH then extracted twice with 1 N HCl (aq). The combined acidic aqueous layers were basified to pH>12 with solid NaOH and extracted 3× with EtOAc. The EtOAc layers were washed once with 2 N NaOH then once with a mixture of brine and 2 N NaOH, combined, dried over Na2SO4, filtered, and concentrated down to dryness, to yield the title compound.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07531553B2
Source datasetuspto-grants-2009_05
ORD IDord-8ff3dc4c17894f27a5c1c35271dc5581
Source noteuspto-grants-2009_05