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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1663458Generated: October 28, 2026

Sodium Hydroxide → HCID 86613753, compound

https://huagongshe.com/reaction/1663458

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSodium HydroxideHCID 14798—
Reactant5-Bromothiazol-2-amine monohydrobromideHCID 2723848—
Reactant3-EthoxythiophenolHCID 2736350—
SolventTetrahydrofuranHCID 8028—
ProductHCID 86613753HCID 8661375380.5%

Reaction Steps

Part A: A mixture of 3-ethoxythiophenol (10.0 g, 0.065 mol), 2-amino-5-bromothiazole monohydrobromide (17.7 g, 0.068 mol), 1 M aqueous NaOH (200 mL), and THF (200 mL) was stirred at RT for 15 min. The reaction mixture was warmed to 55° C. over 1 h, cooled to RT and concentrated under reduced pressure to remove THF. The residue was partitioned between EtOAc (ca. 500 mL) and water (ca 100 mL), and the layers were separated. The organic phase was washed with saturated aqueous NaCl (1×200 mL), dried (Na2SO4), and concentrated under reduced pressure to give a solid. The solid was triturated with CH2Cl2:hexanes (ca. 10:1) to provide 5-(3-ethoxy-phenylsulfanyl)-thiazol-2-ylamine (13.2 g, 80%) as a light brown solid. LCMS (m/z): 253 (M+H)+

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08034954B2
Source datasetuspto-grants-2011_10
ORD IDord-ca9ac59a4a23460c95fa88a5579eba21
Source noteuspto-grants-2011_10