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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1799111Generated: October 27, 2026

Oxalyl chloride → 5-(3-Methoxypropyl)-2-phenylthiazole-4-carbonyl chloride

https://huagongshe.com/reaction/1799111

Reaction equation

Participants

RoleNameHCIDCharge
ReactantOxalyl chlorideHCID 65578—
Reactant5-(3-Methoxypropyl)-2-phenylthiazole-4-carboxylateHCID 86660230—
CatalystDimethylformamideHCID 6228—
SolventDichloromethaneHCID 6344—
Product5-(3-Methoxypropyl)-2-phenylthiazole-4-carbonyl chlorideHCID 5855189699.6%

Reaction Steps

Oxalyl chloride (67.2 mmol, 5.9 mL) was slowly added to a room temperature solution of 5-(3-methoxypropyl)-2-phenylthiazole-4-carboxylate (22.4 mmol, 6.2 g) in CH2Cl2 (100 mL). 3 drops of DMF were added and the reaction became homogeneous over ˜20 min. The reaction was stirred for 3 h, then concentrated under reduced pressure. The crude product was dissolved in CH2Cl2 (150 mL) and concentrated under reduced pressure. The crude product was dissolved in EtOAc (150 mL), washed with brine (2×100 mL), dried (MgSO4), and concentrated under reduced pressure to give 5-(3-methoxypropyl)-2-phenylthiazole-4-carbonyl chloride as a tan solid (6.6 g, 99% yield).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08343997B2
Source datasetuspto-grants-2013_01
ORD IDord-ec35ca7f72cf4cb1bcfd409c34040f4b
Source noteuspto-grants-2013_01