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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1900575Generated: October 29, 2026

2-Thiophenecarboxaldehyde → HCID 23369385, compound

https://huagongshe.com/reaction/1900575

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 numberUS05576315
Source datasetuspto-grants-1996_11
ORD IDord-ecc1fceb17e94b1a952921c6b978c15b
Source noteuspto-grants-1996_11