HuagongsheHuagongshe Chemistry Print Report · For research reference only
Chloroacetaldehyde → HCID 21493045, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Chloroacetaldehyde | HCID 33 | — |
| Reactant | Sulfamide | HCID 82267 | — |
| Solvent | Hydrochloric Acid | HCID 313 | — |
| Product | HCID 21493045 | HCID 21493045 | 70% |
Reaction Steps
0.01 mole of sulphamide in 5 ml of concentrated hydrochloric acid are added to 0.012 mole of chloroacetaldehyde, at room temperature whilst stirring. After 5 minutes, the precipitate which has formed is filtered off and washed with ice water, dried and recrystallised from acetone/petroleum ether. 3,7-Di-(chloromethyl)-1,5-dithia-2,4,6,8-tetra-aza-cyclooctane-1,1,5,5-tetraoxide is obtained as colourless crystals of melting point 175° C (decomposition) in a yield of 70% of the theoretical yield.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US03996242 |
| Source dataset | uspto-grants-1976_12 |
| ORD ID | ord-a4085e667849461f86a693df75142e02 |
| Source note | uspto-grants-1976_12 |