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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1637383Generated: November 2, 2026

Triethylamine → HCID 10760500, compound

https://huagongshe.com/reaction/1637383

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTriethylamineHCID 8471—
Reactant2-Bromoethyl chloroformateHCID 78528—
Reactant1,2-Bis(methylsulfonyl)-1-methylhydrazineHCID 130630—
SolventAcetoneHCID 180—
ProductHCID 10760500HCID 10760500—

Reaction Steps

1,2-Bis(methylsulfonyl)-2-(2-bromoethoxycarbonyl)-1-methylhydrazine (compound 8) was synthesized as follows: Triethylamine (1.45 g, 0.014 mol) was added in portions to a stirred solution of 1,2-bis(methylsulfonyl)-1-methylhydrazine (2.02 g, 0.01 mol) and 2-bromoethyl chloroformate (3.49 g, 0.019 mol) in acetone (100 ml) over a period of 15 min. The reaction mixture was stirred for an additional 18 hr, filtered, and the filtrate evaporated to dryness in vacuo. The residue was taken up in chloroform (100 ml) and washed with water (3×20 ml). The chloroform layer was dried over anhydrous magnesium sulfate, filtered, and the filtrate evaporated to dryness. The residue was triturated with petroleum ether until a solid separated. The solid was filtered and recrystallized from ethanol (1.52 g, 43.0%). Mp was approximately 81-82° C. 1H NMR (CDCl3): δ 4.7 and 3.6 (4H, 2t, CH2CH2Br), 3.5, 3.3 and 3.1 (9H, 3s, 2CH3SO2 and NCH3).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06040338
Source datasetuspto-grants-2000_03
ORD IDord-ca28403d03ad4a80b3c5eb01499c9e98
Source noteuspto-grants-2000_03