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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1459400Generated: November 2, 2026

1-Isocyanatoadamantane → HCID 57147682, compound

https://huagongshe.com/reaction/1459400

Reaction equation

Participants

RoleNameHCIDCharge
Reactant1-IsocyanatoadamantaneHCID 2059995—
ReactantLithium diisopropylamideHCID 2724682—
ReactantHCID 18770380HCID 18770380—
SolventTetrahydrofuranHCID 8028—
SolventCyclohexaneHCID 8078—
ProductHCID 57147682HCID 57147682—

Reaction Steps

To a stirred solution of 3-pyridin4-yl-2-pyridin4-ylmethyl-propionic acid methyl ester (24.44 g, 95 mmol) in tetrahydrofuran (300 ml) chilled with a dry ice/acetone bath, lithium diisopropylamide (70 ml of a 1.5M solution in cyclohexane, 105 mmol of lithium diisopropylamide) was added dropwise over 15 minutes. After stirring for 20 minutes, the solution temperature was elevated to -40° C. After 30 minutes of stirring at -40° C., a solution of adamantyl isocyanate (16.92 g, 95 mmol) in tetrahydrofuran (100 ml) was added dropwise over 10 minutes. After 15 minutes stirring, the cooling bath was removed and the reaction was then stirred for 3 hours at ambient temperature. The reaction was then chilled in an ice water bath and glacial acetic acid (14 ml) was added dropwise over 10 minutes. After stirring for 20 minutes at ambient temperature, the solvent was removed in vacuo, and the residue was extracted into water/methylene chloride (300 ml of each). The aqueous phase was extracted three times with 200 ml portions of fresh methylene chloride. The combined organic extracts were dried (anhydrous sodium sulfate), and concentrated in vacuo to an oil (49.6 g).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05854232
Source datasetuspto-grants-1998_12
ORD IDord-8395f7ea29eb4bf08e5b62db69a38d4f
Source noteuspto-grants-1998_12