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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 436767Generated: October 29, 2026

Methanol → HCID 21431238, compound

https://huagongshe.com/reaction/436767

Reaction equation

Participants

RoleNameHCIDCharge
ReactantMethanolHCID 887—
ReactantSodium hydrideHCID 24758—
ReactantIsocyanateHCID 105034—
Reactant1-t-Butylazo-1-isocyanatocyclohexaneHCID 21431172—
SolventWaterHCID 962—
ProductHCID 21431238HCID 21431238—

Reaction Steps

To 30 ml of methanol in a 100 ml 3 neck round bottom flask equipped with a thermometer and magnetic stirrer was slowly added 2.1 grams (0.05 moles) of 57% sodium hydride. After the temperature came back to 25° C., 10.5 grams (0.05 moles) of 1-t-butylazo-1-isocyanatocyclohexane was added dropwise over 5 minutes. There was a 2° C. rise in temperature during the addition. After the addition was complete, the reaction was stirred an additional 30 minutes at room temperature. Gas chromatography indicated that the 1-t-butylazo-1-isocyanatocyclohexane had reacted almost immediately. The reaction mixture was poured into 300 ml water and the product extracted with 100 ml methylene chloride. The methylene chloride extract was separated, washed with water, 100 ml 10% NaHCO3 solution, dried over anhydrous Na2SO4, filtered and the methylene chloride evaporated under reduced pressure to leave 11.0 grams (91% crude yield) of a yellow liquid. The product had a strong carbonyl band at 1730 cm-1 and a sharp NH band at 3400 cm-1 in its infrared spectrum and the isocyanate band at 2225 cm-1 was absent.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04028344
Source datasetuspto-grants-1977_06
ORD IDord-ac2aff191cf647f385c064b4e7fe24c4
Source noteuspto-grants-1977_06