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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2384075Generated: October 26, 2026

(E)-4-(2-methyl-benzothiazol-6-yl)-but-3-enoic acid methyl ester → 4-(2-Methyl-benzothiazol-6-yl)-butyric acid methyl ester

https://huagongshe.com/reaction/2384075

Reaction equation

Participants

RoleNameHCIDCharge
Reactant(E)-4-(2-methyl-benzothiazol-6-yl)-but-3-enoic acid methyl esterHCID 67505910—
CatalystPalladiumHCID 23938—
SolventTetrahydrofuranHCID 8028—
Product4-(2-Methyl-benzothiazol-6-yl)-butyric acid methyl esterHCID 67505708—

Reaction Steps

Next, a solution of (E)-4-(2-methyl-benzothiazol-6-yl)-but-3-enoic acid methyl ester in THF (10 mL) is hydrogenated over 10% Pd/C (22 mg, 10% wet) at 1 atm for 48 hours. The catalyst is filtered through Celite and the solvent is removed under reduced pressure. The residue is purified by flash chromatography (heptane:EtOAc, 2:1) to give 4-(2-methyl-benzothiazol-6-yl)-butyric acid methyl ester. MS 250.4 (M+1).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08263629B2
Source datasetuspto-grants-2012_09
ORD IDord-53f2d3ce3a2d4b97bd49d7b01491772c
Source noteuspto-grants-2012_09