HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1459400Generated: November 2, 2026
1-Isocyanatoadamantane → HCID 57147682, compound
https://huagongshe.com/reaction/1459400
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | 1-Isocyanatoadamantane | HCID 2059995 | — |
| Reactant | Lithium diisopropylamide | HCID 2724682 | — |
| Reactant | HCID 18770380 | HCID 18770380 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Solvent | Cyclohexane | HCID 8078 | — |
| Product | HCID 57147682 | HCID 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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US05854232 |
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| Source dataset | uspto-grants-1998_12 |
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| ORD ID | ord-8395f7ea29eb4bf08e5b62db69a38d4f |
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| Source note | uspto-grants-1998_12 |
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