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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 409888Generated: October 30, 2026

Methanol → Methyl 5-(bromomethyl)thiazole-4-carboxylate

https://huagongshe.com/reaction/409888

Reaction equation

Participants

RoleNameHCIDCharge
ReactantMethanolHCID 887—
ReactantBenzoyl PeroxideHCID 7187—
ReactantThionyl ChlorideHCID 24386—
ReactantN-bromobutanimideHCID 67184—
Reactant5-Methyl-1,3-thiazole-4-carboxylic acidHCID 14109320—
SolventCarbon TetrachlorideHCID 5943—
ProductMethyl 5-(bromomethyl)thiazole-4-carboxylateHCID 66601492—

Reaction Steps

To a mixture of 5-methylthiazole-4-carboxylic acid 3a (0.50 g, 3.49 mmol) in MeOH (15 mL) at 0° C. was added SOCl2 (0.51 mL, 6.99 mmol). The reaction was warmed up to room temperature and then heated to reflux for 8 h. The reaction mixture was cooled to room temperature and concentrated. The residue was dissolved in CH2Cl2 and washed with aq. NaHCO3. The organic solution was dried over Na2SO4 and concentrated. A portion of the resulting mixture (250 mg, 1.59 mmol) was heated to reflux in CCl4 (15 mL) with NBS (311 mg, 1.75 mmol) and benzoyl peroxide (38.5 mg, 0.159 mmol) for 3 h. The reaction mixture was concentrated and purification by flash column chromatography (silica gel, 30% EtOAc/heptane) gave compound 3b (250 mg).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08759533B2
Source datasetuspto-grants-2014_06
ORD IDord-c2ae47cd7eab44fdbe243cffc793f3cf
Source noteuspto-grants-2014_06