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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1788135Generated: November 4, 2026

Triethylamine → HCID 21069869, compound

https://huagongshe.com/reaction/1788135

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTriethylamineHCID 8471—
ReactantSodium SulfiteHCID 24437—
ReactantTert-Butyl hypochloriteHCID 521297—
ReactantHCID 21069870HCID 21069870—
SolventEthanolHCID 702—
ProductHCID 21069869HCID 2106986980%

Reaction Steps

To a cold stirring solution of 3-m-tolyl-3-trifluoromethyl-diaziridine (2.0 g, 10 mmol. prepared using the methods described in Doucet-Personeni C. et al., J. Med. Chem., 2001, 44, 3203 and Nassal, M. Liebigs Ann. Chem. 1983, 1510-1523 or in Stromgaard, K et al., J. Med. Chem., 2002, 45, 4038-46) in ethanol (20 mL) was added triethylamine (1.5 g, 15 mmol). To this mixture was added tert-butyl hypochlorite (3.25 g, 30 mmol), and the mixture stirred for 5 min. This mixture was poured into 10% aqueous sodium sulfite (100 mL), and extracted with ether. The ether extract was washed with brine, dried (MgSO4), filtered and concentrated. The residue was purified by column chromatography (SiO2, pentane) to provide 1.6 g (Yield 80%) of the title compound. 1H NMR (300 MHz, CDCl3) δ ppm: 2.33 (3 H, s) 6.90-7.03 (2 H, m) 7.15-7.31 (2 H, m).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07511037B2
Source datasetuspto-grants-2009_03
ORD IDord-81c87b1311544d9497322a7ff86f5b41
Source noteuspto-grants-2009_03