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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1768772Generated: October 31, 2026

2-Thiophenecarboxaldehyde → HCID 23369385, compound

https://huagongshe.com/reaction/1768772

Reaction equation

Participants

RoleNameHCIDCharge
Reactant2-ThiophenecarboxaldehydeHCID 7364—
ReactantMethyl 3-aminopropanoate hydrochlorideHCID 2734767—
ReactantSodium cyanoborohydrideHCID 5003444—
SolventMethanolHCID 887—
ProductHCID 23369385HCID 2336938530.1%

Reaction Steps

To a stirring 25 mL MeOH solution of 1.40 g (10 mmol) of methyl β-alaninate hydrochloride and 1.34 g (12 mmol) of thiophene carboxaldehyde was added 1.26 g (20 mmol) of NaCNBH3. After 1 hour, 25 mL of saturated KHCO3 was added to the reaction. The reaction mixture was then filtered, and the resulting filtrate was extracted with 50 mL of DCM. The organic layer was treated as described above in Example 7, and the residue was chromatographed to yield 0.60 g (30%) of product. Analysis calculated for C9H13NO2S (M.W. 199.27): C, 54.25; H, 6.58; N, 7.03. Found: C, 54.02; H, 6.63; N, 6.77.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05378840
Source datasetuspto-grants-1995_01
ORD IDord-5a421a4767bf40de8afac2bd9019da22
Source noteuspto-grants-1995_01