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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 323591Generated: October 29, 2026

2-Bromoethanol → 12-(2-bromo-ethoxy)-2,10-dichloro-12H-5,7-dioxa-dibenzo[a,d]cyclooctene

https://huagongshe.com/reaction/323591

Reaction equation

Participants

RoleNameHCIDCharge
Reactant2-BromoethanolHCID 10898—
ReactantPotassium CarbonateHCID 11430—
Reactant12-bromo-2,10-dichloro-12H-5,7-dioxadibenzo[a,d]cycloocteneHCID 22727778—
SolventDichloromethaneHCID 6344—
Product12-(2-bromo-ethoxy)-2,10-dichloro-12H-5,7-dioxa-dibenzo[a,d]cycloocteneHCID 2272788082.4%

Reaction Conditions

Temperature120 °C

Reaction Steps

A mixture of 12-bromo-2,10-dichloro-12H-5,7-dioxa-dibenzo[a,d]cyclooctene (900 mg, 2.5 mmol), 2-bromoethanol (3.75 g, 30 mmol) and potassium carbonate (1.0 g, 7.2 mmol) in dichloromethane (10 mL) was heated at 120° C. for 4 h. The reaction mixture was concentrated in vacuo, added water (25 mL) and the product extracted with ethyl acetate (3×25 mL). The combined organic phases were dried (MgSO4), filtered and evaporated to give 832 mg (82%) of 12-(2-bromo-ethoxy)-2,10-dichloro-12H-5,7-dioxa-dibenzo[a,d]cyclooctene.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06214820B1
Source datasetuspto-grants-2001_04
ORD IDord-99ba4ba9db934e39a62f1dcf95d7d77a
Source noteuspto-grants-2001_04