HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 892003Generated: October 28, 2026
Ethylenediamine → HCID 10431217, compound
https://huagongshe.com/reaction/892003
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Ethylenediamine | HCID 3301 | — |
| Reactant | Sodium borohydride | HCID 4311764 | — |
| Reactant | HCID 10023919 | HCID 10023919 | — |
| Catalyst | Nickel Dichloride | HCID 24385 | — |
| Solvent | Ethanol | HCID 702 | — |
| Product | HCID 10431217 | HCID 10431217 | 57.3% |
Reaction Steps
95% Ethanol (1.0 mL) was added to a slowly stirred mixture of nickel (II) chloride (86 mg, 0.66 mmol) and sodium borohydride (12 mg, 0.33 mmol) under nitrogen. The mixture immediately turned black. After 15 min, ethylenediamine (70 μL, 1.04 mmol) was added. After an additional 15 min, a solution of alkyne 13 (53 mg, 0.13 mmol) in 95% ethanol (1.0 mL) was added. The flask was evacuated and refilled with hydrogen (3×), and the reaction mixture was stirred vigorously under a balloon of hydrogen for 22 h. The mixture was then filtered through celite, washing with MeOH (5 mL) and the filtrate was concentrated in vacuo. Purification of the residue by flash column chromatography on silica (100% CH2Cl2→50% EtOAc/CH2Cl2, gradient) afforded 30 mg (56%) of the title compound (15).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07005442B2 |
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| Source dataset | uspto-grants-2006_02 |
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| ORD ID | ord-25324a0da8ef4e3884d63898f7d82a0c |
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| Source note | uspto-grants-2006_02 |
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