HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1095493Generated: November 3, 2026
Triethylamine → 8-Isocyanato-8-phenyl-1,4-dioxaspiro[4.5]decane
https://huagongshe.com/reaction/1095493
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Triethylamine | HCID 8471 | — |
| Reactant | 8-Phenyl-1,4-dioxaspiro[4.5]decane-8-carboxylic acid | HCID 12286702 | — |
| Reactant | Phosphoric acid diphenylester azide | HCID 66782931 | — |
| Solvent | Anisole | HCID 7519 | — |
| Product | 8-Isocyanato-8-phenyl-1,4-dioxaspiro[4.5]decane | HCID 12595565 | — |
Reaction Steps
8-Phenyl-1,4-dioxaspiro[4.5]decane-8-carboxylic acid (3 g, 11.5 mmol) was initially introduced into anisole (30 ml). The suspension obtained was cooled to a temperature of 0° C. in an ice/sodium chloride bath and triethylamine (2.25 ml, 16 mmol) was added. A clear solutions was formed and was stirred at 0° C. for a further 15 min. Phosphoric acid diphenyl ester azide (2.5 ml, 11.5 mmol) was then added to the mixture in the course of 5 min. The reaction mixture was stirred at 0° C. for 20 min, allowed to come to RT in the course of a further 20 min and then heated in an oil bath at 100° C. (bath temperature) for 2 h. For working up, the anisole was distilled off under an oil pump vacuum. Purification by chromatography was carried out on silica gel with toluene. The desired product was obtained as a crystalline solid with a melting point of 38-41° C. in a yield of 2.7 g (91%).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08138187B2 |
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| Source dataset | uspto-grants-2012_03 |
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| ORD ID | ord-5dcfc37637ef4797ad244cfca0bbf9e4 |
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| Source note | uspto-grants-2012_03 |
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