HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 322083Generated: October 30, 2026
1,2-Dichloroethane → HCID 15521926, compound
https://huagongshe.com/reaction/322083
Participants
| Role | Name | HCID | Charge |
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| Reactant | 1,2-Dichloroethane | HCID 11 | — |
| Reactant | Hydrochloric Acid | HCID 313 | — |
| Reactant | 4-Methylmorpholine | HCID 7972 | — |
| Reactant | Sodium Hydroxide | HCID 14798 | — |
| Reactant | 1-Hydroxybenzotriazole | HCID 75771 | — |
| Reactant | Methanamine, N-methoxy-, hydrochloride (1:1) | HCID 81138 | — |
| Reactant | HCID 69710510 | HCID 69710510 | — |
| Solvent | Ethanol | HCID 702 | — |
| Solvent | Acetonitrile | HCID 6342 | — |
| Product | HCID 15521926 | HCID 15521926 | — |
Reaction Steps
To a solution of 4-8 (5.6 g, 12.8 mmol) in ethanol (50 mL) was added NaOH (15 mL 1M solution in water, 15 mmol). After stirring for 1 h, HCl (15 mL 1M solution in water, 15 mmol) was added, and the mixture evaporated to give an oily residue. The residue was evaporated from ethanol three times, and then from acetonitrile three times, producing a yellow crusty solid which was dried under a vacuum of <2 mm Hg for 2 h. This residue was then slurried in chloroform (5 mL) and acetonitrile (50 mL), and NMM (8.5 mL), N,O-dimethylhydroxylamine hydrochloride (2.5 g, 26 mmol), HOBT (1.7 g, 13 mmol) and EDC (2.4 g, 13 mmol) were added. After stirring for 15 h, the mixture was evaporated to dryness, the residue slurried in EtOAc, washed with sat. NaHCO3, brine, and dried over Na2SO4. Evaporative removal of the solvent gave 4-9 as a yellow oil.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US06211191B1 |
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| Source dataset | uspto-grants-2001_04 |
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| ORD ID | ord-f5f1de93df4949fc88dd1c76af276a0b |
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| Source note | uspto-grants-2001_04 |
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