HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 653005Generated: October 25, 2026
Water → 2-Chloroethyl 2-chloro-N-hydroxybenzenecarboximidothioate
https://huagongshe.com/reaction/653005
Participants
| Role | Name | HCID | Charge |
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| Reactant | Water | HCID 962 | — |
| Reactant | Triethylamine | HCID 8471 | — |
| Reactant | Ethanethiol, 2-chloro- | HCID 78022 | — |
| Reactant | o-Chlorobenzaldoxime | HCID 96239 | — |
| Solvent | Diethyl Ether | HCID 3283 | — |
| Solvent | Chloroform | HCID 6212 | — |
| Product | 2-Chloroethyl 2-chloro-N-hydroxybenzenecarboximidothioate | HCID 73184959 | — |
Reaction Steps
2-Chlorobenzaldoxime (46.7 g, 0.3 mol) in chloroform (350 ml) was cooled and stirred in an ice/salt bath. Chlorine gas was bubbled into the reaction until an excess was present. Excess chlorine and solvent were removed and the remaining 2-chloro-N-hydroxybenzenecarboximidoyl chloride dissolved in ether (250 ml). Solutions of triethylamine (30.3 g, 0.3 mol) in ether (50 ml) and 2-chloroethanethiol (29 g, 0.3 mol) in ether (50 ml) were added simultaneously with stirring and cooling. After the addition, the reaction was allowed to warm to room temperature and left overnight. Water was added, and the ether layer was washed with additional water, then dried with anhydrous magnesium sulphate. Evaporation left a white solid, 2-chloroethyl 2-chloro-N-hydroxybenzenecarboximidothioate, m.p. 115°-117° C., (Found: C, 43.29; H, 3.58; N, 5.59. C9H9Cl2NOS requires C, 43.21; H, 3.62; N, 5.60).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US04675044 |
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| Source dataset | uspto-grants-1987_06 |
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| ORD ID | ord-5604cb1c320e49fcaabd983b04feefc9 |
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| Source note | uspto-grants-1987_06 |
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