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
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Acetic Anhydride | HCID 7918 | — |
| Reactant | Triethylamine | HCID 8471 | — |
| Reactant | VPN-4090CE | HCID 10198873 | — |
| Solvent | Acetone | HCID 180 | — |
| Product | 1-Acetyl-1,2-bis(methylsulfonyl)-2-(2-chloroethyl)hydrazine | HCID 3025822 | 62.8% |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US05256820 |
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| Source dataset | uspto-grants-1993_10 |
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| ORD ID | ord-103f8d386bb24d57bd3b91c0d79748e9 |
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| Source note | uspto-grants-1993_10 |
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