HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1942412Generated: November 3, 2026
Triethylamine → N-(indan-2-yl)-5-oxopentanamide
https://huagongshe.com/reaction/1942412
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Triethylamine | HCID 8471 | — |
| Reactant | Oxalyl chloride | HCID 65578 | — |
| Reactant | N-(indan-2-yl)-5-hydroxypentanamide | HCID 66937348 | — |
| Solvent | Dimethyl Sulfoxide | HCID 679 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Solvent | Sodium chloride; water | HCID 57417360 | — |
| Product | N-(indan-2-yl)-5-oxopentanamide | HCID 86651316 | — |
Reaction Steps
A solution of 1.11 mL (12.8 mmol) oxalyl chloride in 35 mL of dichloromethane is cooled to −80° C. under argon atmosphere. 2.33 mL (32.7 mmol) of dimethylsulfoxide in 9.33 mL of dichloromethane is introduced dropwise over 10 minutes. After 5 minutes a solution of 1.63 g (7 mmol) N-(2,3-dihydro-1H-inden-2-yl)-5-hydroxypentanamide in 8 mL dichloromethane and 2 mL dimethylsulfoxide is added over the course of 10 minutes. The reaction mixture is stirred for another hour at −80° C. before 5 mL of triethylamine is added and the mixture is allowed to warm up to room temperature. 50 mL of saturated brine solution is added for hydrolysis. The organic phase is separated, extracted three times with a saturated solution of sodium chloride, dried over sodium sulfate and the solvent is evaporated.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08389555B2 |
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| Source dataset | uspto-grants-2013_03 |
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| ORD ID | ord-b2d19534dd624f0aa8113c3699c51111 |
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| Source note | uspto-grants-2013_03 |
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