HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2072504Generated: October 30, 2026
Triethylamine → 8-(1H-Indene-2-carbonyl)-1-phenyl-1,3,8-triazaspiro[4.5]decan-4-one
https://huagongshe.com/reaction/2072504
Participants
| Role | Name | HCID | Charge |
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| Reactant | Triethylamine | HCID 8471 | — |
| Reactant | Ethyl chloroformate | HCID 10928 | — |
| Reactant | 1-Phenyl-1,3,8-triazaspiro(4.5)decan-4-one | HCID 70556 | — |
| Reactant | 1H-Indene-2-carboxylic acid | HCID 575464 | — |
| Catalyst | 4-Methylmorpholine | HCID 7972 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | 8-(1H-Indene-2-carbonyl)-1-phenyl-1,3,8-triazaspiro[4.5]decan-4-one | HCID 21408248 | — |
Reaction Steps
Indene-2-carboxylic acid (12.8g) is dissolved in dry tetrahydrofuran (300 ml), cooled to 0° C, treated with N-methylmorpholine (40 drops), triethylamine (12 ml) and ethyl chloroformate (8.6g) and stirred for 30 minutes. To this mixture is added a suspension of 1-phenyl-1,3,8-triazaspiro[4.5]decan-4-one (20.0g) in dry tetrahydrofuran (200 ml) and the mixture is stirred at 0° C for 30 minutes. The mixture is allowed to warm to room temperature and stirred for 16 hours. The precipitated solids are filtered off, washed with additional tetrahydrofuran, and the filtrate is concentrated. The semi-solid residue is dissolved in chloroform, washed with water and saturated sodium bicarbonate solution, dried, and concentrated to give the crude product.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US04051248 |
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| Source dataset | uspto-grants-1977_09 |
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| ORD ID | ord-eafd6a170e7c408f9703229bf0c3c81c |
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| Source note | uspto-grants-1977_09 |
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