HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 460336Generated: October 30, 2026
1-Indanone → 1H-Indene-2-carbothioamide, 2,3-dihydro-1-oxo-N-phenyl-
https://huagongshe.com/reaction/460336
Participants
| Role | Name | HCID | Charge |
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| Reactant | 1-Indanone | HCID 6735 | — |
| Reactant | Phenyl Isothiocyanate | HCID 7673 | — |
| Reactant | Sodium hydride | HCID 24758 | — |
| Reactant | Ammonium Chloride | HCID 25517 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | 1H-Indene-2-carbothioamide, 2,3-dihydro-1-oxo-N-phenyl- | HCID 10967488 | — |
Reaction Steps
NaH (60% dispersion in mineral oil, 0.25 g, 6 mmol) and indan-1-one, Compound 1a, (0.50 g, 3.79 mmole) in THF (5 mL) were mixed under argon. The mixture was stirred at ambient temperature for 5 min. Then, phenylisothiocyanate, Compound 1b, (0.46 mL, 3.79 mmole) was added to the mixture. After an additional 5 min, the reaction was completed as shown by TLC analysis and the reaction mixture was poured into NH4Cl solution and then filtered subsequently. 1-Oxo-indan-2-carbothioic acid phenylamide (Intermediate A), was crystallized from CH3CN as a yellow solid. MS m/z 268 (M+H)+; 1H NMR (DMSO-d6):3.5 (dd, 0.3H), 3.8 (d, 0.15H), 3.9 (s, 1.55H), 4.3 (dd, 0.3H), 7.3 (t, 1H), 7.4–7.8 (m, 7.4H), 7.9 (d, 0.6H), 10.6 (s, 0.7H), 12.1 (s, 0.3H), 14.1 (s, 0.7H).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07196110B2 |
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| Source dataset | uspto-grants-2007_03 |
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| ORD ID | ord-d4fc242a2e9540f1ab6f2a40ca693b2c |
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| Source note | uspto-grants-2007_03 |
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