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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 732244Generated: October 26, 2026

Acetic Acid → 4-(5-Isopropyl-2-Methyl-1,3-Thiazol-4-Yl)-Phenol

https://huagongshe.com/reaction/732244

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAcetic AcidHCID 176—
ReactantPotassium CarbonateHCID 11430—
ReactantBromic acidHCID 24445—
Reactant5-Isopropyl-4-(4-Methoxy-Phenyl)-2-Methyl-1,3-ThiazoleHCID 57838363—
SolventDichloromethaneHCID 6344—
Product4-(5-Isopropyl-2-Methyl-1,3-Thiazol-4-Yl)-PhenolHCID 1620244484.1%

Reaction Steps

While 35.8 g of 5-isopropyl-4-(4-methoxy-phenyl)-2-methyl-1,3-thiazol (5) prepared in Example 3 were added to 86 ml of acetic acid and stirred, 500 ml of 48% bromic acid were added. Subsequently, the temperature was gradually increased and stirring under reflux was continued for 18 hr. The temperature was decreased to room temperature, and 400 ml of dichloromethane were added and stirring was further continued for 30 min. Then, the dichloromethane layer was removed. Thereafter, the obtained reaction solution was added with a saturated aqueous solution of potassium carbonate to be neutralized at pH 7-8, after which the precipitated solid was filtered and then washed with water, thus obtaining 28.4 g (yield: 84%) of a title compound as a solid.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07585979B2
Source datasetuspto-grants-2009_09
ORD IDord-99e28f6d90aa4fec9a62e66e94631da9
Source noteuspto-grants-2009_09