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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 366439Generated: October 29, 2026

2-Bromothiazole → HCID 23289316, compound

https://huagongshe.com/reaction/366439

Reaction equation

Participants

RoleNameHCIDCharge
Reactant2-BromothiazoleHCID 76430—
Reactant2-BenzyloxyphenolHCID 80459—
SolventDimethylformamideHCID 6228—
ProductHCID 23289316HCID 2328931648.9%

Reaction Conditions

Temperature100 °C

Reaction Steps

o-Benzyloxyphenol (7.5 g, 37.5 mmol) in dry DMF (60 mL) was treated with Me4N+OH-.5H2O (37.5 mmol, 6.8 g) followed by 2-bromothiazole (6.15 g, 37.5 mmol). The stirred solution was heated to about 100° C. under N2 (g) for 16 hours. The mixture was cooled in ice and crystalline, H2O-soluble Me4N+Br- was removed by filtration. The filtrate was concentrated in vacuo and partitioned between Et2O (100 mL) and H2O (60 mL). The organic phase was washed with 1N NaOH (3×) and brine, dried over Na2SO4 and concentrated in vacuo to afford 4.9 g of crude 2-(2-benzyloxyphenyl)thiazole (GCMS m/z 283 (M+)). This material was directly deprotected by treatment with 33% HBr in HOAc (35 mL) for 2 hours at about 20° C.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06130217
Source datasetuspto-grants-2000_10
ORD IDord-b1771c7c193346fa839da4ae35ad19b2
Source noteuspto-grants-2000_10