HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 623304Generated: October 29, 2026
Propyl isocyanate → HCID 123792055, compound
https://huagongshe.com/reaction/623304
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Propyl isocyanate | HCID 61033 | — |
| Reactant | Potassium tert-butoxide | HCID 23665647 | — |
| Reactant | HCID 131735176 | HCID 131735176 | — |
| Solvent | Acetonitrile | HCID 6342 | — |
| Product | HCID 123792055 | HCID 123792055 | 32% |
Reaction Steps
5 ml of anhydrous acetonitrile was added to 11 mg (0.13 mmol) of normal propyl isocyanate, 40 mg (0.12 mmol) of the N-[1-((6-chloropyridin-3-yl)methyl)pyridin-2(1H)-ylidene]-2,2,2-trifluoro-N′-hydroxyacetimidamide (1-499) synthesized by the method in Synthetic Example 7 and 4 mg (0.04 mmol) of potassium-t-butoxide were added thereto, and the resulting mixture was stirred at room temperature for 1 hour. After the reaction was completed, the reaction solution was concentrated under reduced pressure, and ethyl acetate and a saturated saline solution were added thereto to perform liquid separation. The ethyl acetate layer was dried over anhydrous magnesium sulfate, concentrated under reduced pressure and purified by a TLC plate (one sheet of 0.5 mm plate, evolved with hexane:ethyl acetate=1:3) to obtain the subject material. Amount obtained 16 mg (yield 32%).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US09301525B2 |
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| Source dataset | uspto-grants-2016_04 |
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| ORD ID | ord-684e078cbfe846fa8b55566072898f00 |
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| Source note | uspto-grants-2016_04 |
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