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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2271502Generated: October 30, 2026

Acetic Acid → HCID 86722615, compound

https://huagongshe.com/reaction/2271502

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAcetic AcidHCID 176—
ReactantFormaldehydeHCID 712—
ReactantTriethylamineHCID 8471—
ReactantSodium HydroxideHCID 14798—
ReactantHCID 70676475HCID 70676475—
ReactantHCID 131733375HCID 131733375—
SolventMethanolHCID 887—
ProductHCID 86722615HCID 8672261561%

Reaction Steps

Triethylamine (0.2 mL, 1.4 mmol) was added to 3-(naphthalen-2-yl(phenoxy)methyl)azetidine hydrochloride (0.3 g, 0.92 mmol) dissolved in the methanol solution (20 mL), and stirred at room temperature for 1 hour. Formaldehyde (37% aqueous solution, 0.32 mL, 3.7 mmol), acetic acid (0.21 mL, 3.7 mmol) and sodium acetate borohydride (0.78 g, 3.7 mmol) were added in this order to the reaction mixture, and heated to reflux for one day. The temperature was reduced to room temperature, and 1N caustic soda solution (10 mL) was added thereto, followed by stirring for 30 minutes. The reaction mixture was extracted with methylene chloride, and the organic layer was washed with distilled water once, and then dried over anhydrous magnesium sulfate. The solvent was removed by reduced pressure evaporation to obtain a light yellow oily liquid, which was purified by flash chromatography (methylene chloride:methanol=9:1) to obtain a light yellow oily liquid (0.17 g).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09120771B2
Source datasetuspto-grants-2015_09
ORD IDord-289ec11016fa41268f728b5f48478230
Source noteuspto-grants-2015_09