HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2269603Generated: November 1, 2026
1,2-Dichloroethane → HCID 131721924, compound
https://huagongshe.com/reaction/2269603
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | 1,2-Dichloroethane | HCID 11 | — |
| Reactant | Ammonium Chloride | HCID 25517 | — |
| Reactant | 1-Hydroxybenzotriazole | HCID 75771 | — |
| Reactant | HCID 131721919 | HCID 131721919 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Product | HCID 131721924 | HCID 131721924 | 85.9% |
Reaction Steps
Boc-Gly-Pro-Nleu-OH (4.1 g, 0.0106 mol.), NH4Cl (1.7 g, 0.032 mol.) and HOBt (1.76 g, 0.013 mol.) were dissolved in 100 ml DMF and the solution was chilled to 0° C. TEA (4.5 ml) was added to the solution slowly while stirring the solution. After a while, EDC (2.6 g, 0.013 mol.) was added to the solution. The stirring was continued overnight. The DMF was removed under reduced pressure and the resulting mixture was poured into 350 ml chloroform. The chloroform solution was washed by H2O 2×20 ml, saturated NaHCO3 2×20 ml, brine 2×20 ml, saturated NaHSO4 2×20 ml and brine again until the pH of the brine layer was approximate 7. The organic layer was dried using Na2SO4 and the chloroform was distilled under reduced pressure to obtain the product (3.5 g, 84%). TLC Rf=0.36 (developing solvents: CMA, 85:15:3).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US06329506B1 |
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| Source dataset | uspto-grants-2001_12 |
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| ORD ID | ord-65586d2082a64f72a1a6b14e84ad39f7 |
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| Source note | uspto-grants-2001_12 |
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