HuagongsheHuagongshe Chemistry Print Report · For research reference only
Ethoxalyl chloride → 1-Ethyl-1-ethoxalyl-thiosemicarbazide
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Ethoxalyl chloride | HCID 20884 | — |
| Reactant | 2-Ethylhydrazinecarbothioamide | HCID 22105028 | — |
| Solvent | Acetone | HCID 180 | — |
| Product | 1-Ethyl-1-ethoxalyl-thiosemicarbazide | HCID 20558125 | — |
Reaction Steps
Ethoxalyl chloride (10.6 cc) is added dropwise, in the course of 10 minutes, to a solution, at 20° C., of 1-ethyl-thiosemicarbazide (11.9 g) in acetone (200 cc). The temperature rises to 43° C., the mixture is stirred for 1 hour without heating and is concentrated to dryness at 20° C. under 20 mm Hg (2.7 kPa), the residue is taken up in methanol (30 cc) and the crystallisation is started. After filtration and drying, 1-ethyl-1-ethoxalyl-thiosemicarbazide (13.2 g) is obtained in the form of a white solid melting at 170° C.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04307116 |
| Source dataset | uspto-grants-1981_12 |
| ORD ID | ord-c40b265242454c35a03a82b06c881f90 |
| Source note | uspto-grants-1981_12 |