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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 623304Generated: October 29, 2026

Propyl isocyanate → HCID 123792055, compound

https://huagongshe.com/reaction/623304

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPropyl isocyanateHCID 61033—
ReactantPotassium tert-butoxideHCID 23665647—
ReactantHCID 131735176HCID 131735176—
SolventAcetonitrileHCID 6342—
ProductHCID 123792055HCID 12379205532%

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

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09301525B2
Source datasetuspto-grants-2016_04
ORD IDord-684e078cbfe846fa8b55566072898f00
Source noteuspto-grants-2016_04