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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1657231Generated: November 1, 2026

Acetic Anhydride → 1-Acetyl-1,2-bis(methylsulfonyl)-2-(2-chloroethyl)hydrazine

https://huagongshe.com/reaction/1657231

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAcetic AnhydrideHCID 7918—
ReactantTriethylamineHCID 8471—
ReactantVPN-4090CEHCID 10198873—
SolventAcetoneHCID 180—
Product1-Acetyl-1,2-bis(methylsulfonyl)-2-(2-chloroethyl)hydrazineHCID 302582262.8%

Reaction Steps

To a stirred solution of 1,2-bis(methylsulfonyl)-1-(2-chloroethyl)hydrazine (1.5 g, 0.006 mol) and acetic anhydride (4.3 g, 0.042 mol) in dry acetone (50 mL), triethylamine (3.6 g, 0.035 mol) was added dropwise at room temperature. After an additional 16 h, the reaction mixture was evaporated to dryness. The residue was taken up in ethyl acetate (50 mL) and washed with dilute hydrochloric acid (3×10 mL), followed by water (3×10 mL). The ethyl acetate layer was dried over anhydrous magnesium sulfate, treated with charcoal and filtered. On evaporation of the solvent a solid was obtained which, on recrystallization from ethanol, gave 1.1 g (62.8%) of the title compound: mp 148°-149° C.; 1H NMR (acetone-d6) δ 3.8-4.2 (m, 4 H, CH2CH2), 3.5 and 3.3 (2 s, 6 H, 2CH3SO 2), 2.4 (s, 3 H, CH3CO). Anal. (C6H13C1N2O5S2) C, H, N.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05256820
Source datasetuspto-grants-1993_10
ORD IDord-103f8d386bb24d57bd3b91c0d79748e9
Source noteuspto-grants-1993_10