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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

Reaction equation

Participants

RoleNameHCIDCharge
Reactant1-IndanoneHCID 6735—
ReactantPhenyl IsothiocyanateHCID 7673—
ReactantSodium hydrideHCID 24758—
ReactantAmmonium ChlorideHCID 25517—
SolventTetrahydrofuranHCID 8028—
Product1H-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

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07196110B2
Source datasetuspto-grants-2007_03
ORD IDord-d4fc242a2e9540f1ab6f2a40ca693b2c
Source noteuspto-grants-2007_03