HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1904155Generated: October 25, 2026
1,1-Dichloroethane → HCID 14816499, compound
https://huagongshe.com/reaction/1904155
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | 1,1-Dichloroethane | HCID 6365 | — |
| Reactant | Trinitromethane | HCID 10602 | — |
| Reactant | Bis(iodomethyl)ether | HCID 598725 | — |
| Reactant | HCID 14816496 | HCID 14816496 | — |
| Solvent | 1,2-Dichloroethane | HCID 11 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | HCID 14816499 | HCID 14816499 | — |
Reaction Steps
As illustrated by example 3, a dry solution of nitroform in a suitable inert organic solvent such as methylene chloride, 1,1-dichloroethane, 1,2-dichloroethane, 1,1,2-dichloroethane, etc., is added slowly to the iodomethyl 2-(trimethylsilyloxy)ethyl ether solution while the temperature of the solution is maintained in the range of from -50° C. to -80° C., and preferably from -70° C. to -80° C. Next, dry dimethylformamide is added to ionize the nitroform so that it will react with the iodomethyl ether. The solution is then allowed to warm slowly to a temperature of from about -5° C. to about +5° C. where it is kept until the reaction is completed. Pouring into ice water and then extraction into an organic solvent (e.g., methylene chloride) yields a crude 2,2,2-trinitroethyl 2-hydroxyethyl ether mixture.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | USH0000644 |
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| Source dataset | uspto-grants-1989_06 |
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| ORD ID | ord-c558b83156cb41f988a703a2916fb86a |
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| Source note | uspto-grants-1989_06 |
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