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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2271498Generated: November 2, 2026

Acetic Acid → HCID 86722609, compound

https://huagongshe.com/reaction/2271498

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAcetic AcidHCID 176—
ReactantFormaldehydeHCID 712—
ReactantTriethylamineHCID 8471—
ReactantSodium HydroxideHCID 14798—
ReactantSodium triacetoxyborohydrideHCID 5049666—
ReactantHCID 70676330HCID 70676330—
SolventMethanolHCID 887—
ProductHCID 86722609HCID 86722609—

Reaction Steps

Triethylamine (0.2 mL, 1.313 mmol) was added to 20 mL of 3-((3,4-dichlorophenyl)(phenoxy)methyl)azetidine hydrochloride (300 mg, 0.870 mmol) dissolved in a methanol solution, and the mixture was stirred at room temperature for 1 hour. 37% formaldehyde aqueous solution (0.3 ml, 3.50 mmol) and acetic acid (0.2 ml, 3.50 mmol) were added to the reaction mixture, and NaBH(OAc)3 (742 mg, 3.50 mmol) was added thereto, followed by stirring for one day. Thereafter, 1 mL of 1 N NaOH was added thereto, and the mixture was stirred for 30 minutes. The organic layer was washed with distilled water, and the organic layer was adjusted to pH 7 using a 1 N NaOH aqueous solution, and extracted with methylene chloride (3*30 mL) and dried over anhydrous magnesium sulfate. The solvent was removed by reduced pressure evaporation to obtain a colorless liquid, which was purified by flash chromatography (methylene chloride:methanol (9:1, v/v)). The product was identified as a single compound by TLC (methylene chloride:methanol (9:1, v/v)).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09120771B2
Source datasetuspto-grants-2015_09
ORD IDord-b7f84c681cae46b08c1c88296b9dc7f3
Source noteuspto-grants-2015_09