Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1242003Generated: October 28, 2026

1-Bromo-2-Chloroethane → 5-(2-Chloroethoxy)-2-methylthio-benzothiazole

https://huagongshe.com/reaction/1242003

Reaction equation

Participants

RoleNameHCIDCharge
Reactant1-Bromo-2-ChloroethaneHCID 7849—
ReactantPotassium CarbonateHCID 11430—
Reactant5-Benzothiazolol,2-(methylthio)-(9CI)HCID 21937628—
SolventDimethylformamideHCID 6228—
Product5-(2-Chloroethoxy)-2-methylthio-benzothiazoleHCID 2193748746%

Reaction Conditions

Temperature70 °C

Reaction Steps

To a solution of 5-hydroxy-2-methylthio-benzothiazole (2.1 g, 11 mmol) in anhydrous DMF (25 mL) was added bromo-2-chloroethane (4.4 mL, 53 mmol) and powdered K2CO3 (7.3 g, 53 mmol). The reaction slurry was heated at 70° C. for 13 h. The slurry was filtered under vacuum and the filtrate was concentrated under reduced pressure. The crude material was chromatographed (SiO2, 0–20% EtOAc/Hex) to afford the title compound (1.2 g, 46%). 1H-NMR (CDCl3): δ 7.62 (1H, d), 7.39 (1H, d), 6.97 (1H, dd), 4.29 (2H, t), 3.85 (2H, t), 2.79 (3H, s); MS(ESI): 259(MH+).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07115640B2
Source datasetuspto-grants-2006_10
ORD IDord-f87b3f7d025b42ba981202e81a52169e
Source noteuspto-grants-2006_10