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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1057770Generated: November 2, 2026

Diethyl Ether → HCID 10303191, compound

https://huagongshe.com/reaction/1057770

Reaction equation

Participants

RoleNameHCIDCharge
ReactantDiethyl EtherHCID 3283—
ReactantDiisopropylethylamineHCID 81531—
ReactantHCID 12967649HCID 12967649—
ReactantHCID 21916307HCID 21916307—
SolventDichloromethaneHCID 6344—
ProductHCID 10303191HCID 1030319194%

Reaction Steps

A stirred suspension of benzyl-3,3,3-trifluoropropyl-amine hydrochloride (152.8 mg, 3 equiv.) in methylene chloride (10 mL) at room temperature was treated with diisopropylethylamine (0.132 mL, 3 equiv.). Within a few minutes the mixture became homogeneous and then a 12.5 mg/mL solution of (5-chloromethyl-4-trifluoromethyl-thiazol-2-yl)-(2,4,6-trichloro-phenyl)-amine in ether (8 mL, 0.2525 mmoles) was added all at once. After 12 hours at room temperature, the mixture was evaporated and the residue partitioned between ethyl acetate and water. The organic phase was washed with brine, dried over sodium sulfate and evaporated. The residue was chromatographed on silica gel, eluting with 12% ethyl acetate/hexane, to give the product as a colorless glass (133.6 mg, 94%). 1H-NMR δ (CDCl3) 2.27 (m, 2H), 2.75 (ABq, 2H), 3.62 (s, 2H), 3.74 (s, 2H), 7.28 (m, 5H), 7.48 (s, 2H), 8.75 (br, 1H). Mass spec.: 563.98 (MH+).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06515005B2
Source datasetuspto-grants-2003_02
ORD IDord-14917b90d83b44d3ab31a02824fae4b7
Source noteuspto-grants-2003_02