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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 500688Generated: October 30, 2026

Acetic Acid → HCID 59424239, compound

https://huagongshe.com/reaction/500688

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAcetic AcidHCID 176—
Reactant4-MethoxybenzylamineHCID 75452—
ReactantSodium triacetoxyborohydrideHCID 5049666—
ReactantHCID 57443972HCID 57443972—
Solvent1,2-DichloroethaneHCID 11—
ProductHCID 59424239HCID 59424239—

Reaction Steps

Ethyl 6-acetyl-1-benzothiophene-2-carboxylate (0.3 g, 1.21 mmol) was dissolved in DCE (3.0 mL). 4-methoxybenzyl amine was then added to the reaction followed by acetic acid (0.1 mL, 1.69 mmol) and NaBH(OAc)3 (0.41 g, 1.93 mmol). The reaction was allowed to stir for 5 d at room temperature before it was quenched with saturated sodium bicarbonate solution. The reaction mixture was then extracted with ethyl acetate (3×) and the combined organic layers was dried over Na2SO4. After concentrating in vacuo, the crude reaction mixture was purified by flash column chromatography to provide the amine. 1H (600 MHz, CDCl3) δ 8.03 (s, 1H), 7.84 (s, 1H), 7.82 (s, 1H), 7.41 (d, J=8.9 Hz, 1H), 7.18 (d, J=8.5 Hz, 2H), 6.85 (d, J=8.5 Hz, 2H), 4.40 (q, J=7.1 Hz, 2H), 3.93 (q, J=6.5 Hz, 1H), 3.79 (s, 3H), 3.57 (dd, J=21.0, 12.9 Hz, 2H), 1.42-1.26 (m, 6H). MS: cal'd (MH+) 370, exp (MH+) 370.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07772238B2
Source datasetuspto-grants-2010_08
ORD IDord-e1af59b6692f48949f7858e7b20ed033
Source noteuspto-grants-2010_08