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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 329770Generated: October 26, 2026

Dichloromethane → 2-(2-Aminoethoxy)-1,3,5-trichlorobenzene

https://huagongshe.com/reaction/329770

Reaction equation

Participants

RoleNameHCIDCharge
ReactantDichloromethaneHCID 6344—
ReactantTriethylamineHCID 8471—
ReactantBromoacetyl bromideHCID 61147—
ReactantN-(2-(2,4,6-Trichlorophenoxy)ethyl)-1-propanamineHCID 3842173—
SolventWaterHCID 962—
Product2-(2-Aminoethoxy)-1,3,5-trichlorobenzeneHCID 7139321—

Reaction Conditions

Temperature-70 °C

Reaction Steps

N-(n-propyl) ethanolamine 2,4,6-trichlorophenylether, 11.3 gm, was added to 100 ml of methylene chloride. 5.6 ml of triethylamine was added to the system. The system was stirred at about -70° C for 5 minutes and then 3.5 ml of α-bromoacetyl bromide was added dropwise. The system was stirred at room temperature for an additional 18 hours. The reaction was stopped and the system poured into 100 ml of water. The product was extracted with methylene chloride. The organic solution was dried over magnesium sulfate and the methylene chloride was then removed by stripping to give the N-(α-bromoacetyl), N-(npropyl) ethanolamine 2,4,6-trichlorophenylether as a brown oil. Listed as Compound No. 3 in Table I.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04892952
Source datasetuspto-grants-1990_01
ORD IDord-5caa79e9974244b2af0015179e757dba
Source noteuspto-grants-1990_01