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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 655535Generated: October 31, 2026

Acetic Acid → HCID 67080067, compound

https://huagongshe.com/reaction/655535

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAcetic AcidHCID 176—
ReactantSulfuric acid magnesium salt (1:1)HCID 24083—
ReactantAcetaldehyde, 2,2-dimethoxy-HCID 162650—
ReactantSodium cyanoborohydrideHCID 5003444—
ReactantHCID 67080110HCID 67080110—
SolventMethanolHCID 887—
ProductHCID 67080067HCID 6708006784.1%

Reaction Conditions

Temperature0 °C

Reaction Steps

To a solution of (S)-3-benzyloxy-1-methoxymethyl-propylamine (1.34 g, 6.40 mmol) in methanol (25 mL) were added dimethoxyacetaldehyde solution (45% in tert-butyl methyl ether, 1.81 mL, 7.04 mmol), magnesium sulfate (6.94 g, 57.6 mmol), acetic acid (1.54 g, 25.6 mmol), and sodium cyanoborohydride (551 mg, 8.32 mmol), then after 4 h the reaction mixture was cooled to 0° C. and treated with another portion of dimethoxyacetaldehyde solution (45% in tert-butyl methyl ether, 0.22 mL, 0.96 mmol). The ice bath was removed, then after 2 h the reaction was stopped by careful addition of sat. aq. sodium hydrogencarbonate solution. The reaction mixture was partitioned between sat. aq. sodium hydrogencarbonate solution and ethyl acetate, the organic layer was washed with brine, dried (MgSO4), filtered, and evaporated. Chromatography (SiO2; dichloromethane/methanol 19:1) furnished the title compound (1.60 g, 84%). Light yellow liquid, MS (ISP)=298.3 (M+H)+.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08071586B2
Source datasetuspto-grants-2011_12
ORD IDord-2191bd84e68f4937a3d5e347cd3a34e7
Source noteuspto-grants-2011_12