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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1464443Generated: October 31, 2026

Acetaldehyde → HCID 131718396, compound

https://huagongshe.com/reaction/1464443

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAcetaldehydeHCID 177—
ReactantWaterHCID 962—
ReactantAcetonitrileHCID 6342—
ReactantSodium cyanoborohydrideHCID 5003444—
ReactantHCID 15293134HCID 15293134—
SolventAcetic AcidHCID 176—
ProductHCID 131718396HCID 131718396—

Reaction Steps

To a stirred solution of the title compound of Example 13 (2.0 g), acetaldehyde (3.0 mL), sodium cyanoborohydride (0.904 g), and water (2.6 mL) in acetonitrile (20 mL) was added glacial acetic acid (0.5 mL) over a period of 6 minutes. The reaction was stirred for 2.5 hours at ambient temperature, and then glacial acetic acid was added (0.5 mL), and the reaction was stirred for an additional 30 minutes. The resulting mixture was evaporated under vacuum, and the residue was partitioned between ethyl acetate and saturated sodium bicarbonate. The layers were separated, and the aqueous layer was extracted once more with ethyl acetate. The combined ethyl acetate extracts were washed with brine, dried over magnesium sulfate, and evaporated under vacuum to a clear, greenish oil. The oil was chromatographed four times:twice through silica gel 60 using 97:3 ethyl acetate:ethanol; next through silica gel 60 using 3:1 chloroform:tetrahydrofuran; and finally through reverse phase silica gel (C18) using 80:20:1 acetonitrile:water:ammonium hydroxide. The product from the last column was co-evaporated three times with ethanol to azeotrope water from the product and dried under vacuum at room temperature to yield the title compound as a white solid containing 1.86% water. HPLC: 99.53% pure.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05304644
Source datasetuspto-grants-1994_04
ORD IDord-cc2addb763b24e89ac288c0543b482f5
Source noteuspto-grants-1994_04