HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1408799Generated: November 1, 2026
Bis(trimethylsilyl)carbodiimide → HCID 178423821, compound
https://huagongshe.com/reaction/1408799
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Bis(trimethylsilyl)carbodiimide | HCID 70473 | — |
| Reactant | 3-(2-(2,2-dimethyltetrahydro-2H-pyran-4-yl)-4-oxochroman-6-yl)benzonitrile | HCID 67174832 | — |
| Catalyst | Titanium Tetrachloride | HCID 24193 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | HCID 178423821 | HCID 178423821 | 103.8% |
Reaction Steps
To a solution of 3-(2-(2,2-dimethyltetrahydro-2H-pyran-4-yl)-4-oxochroman-6-yl)benzonitrile (251 mg, 0.69 mmol) in anhydrous DCM (15 mL) under N2 atmosphere was added 1 M TiCl4 (in DCM, 1.4 mL, 1.4 mmol) dropwise within 5 min at room temperature. It was stirred another 1 h after the addition. To this mixture was added Bis-trimethylsilylcarbodiimide (283 mg, 340 μL 1.52 mmol) dropwise. The resulting mixture was stirred for another 20 h after the addition. The reaction mixture was poured into ice-water (20 g), It was transferred to a separating funnel after stirred for 30. The separated aqueous phase was extracted with DCM (2×20 mL). The combined organic phases were dried over anhydrous Na2SO4, and filtered, and concentrated to give yellowish gel like solid (E)-N-(6-(3-cyanophenyl)-2-(2,2-dimethyltetrahydro-2H-pyran-4-yl)chroman-4-ylidene)cyanamide (276 mg), which was used for next step without further purification. MS ESI+ve m/z 386 (M+H)+.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08921359B2 |
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| Source dataset | uspto-grants-2014_12 |
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| ORD ID | ord-dc552f5b07fa471e80a1d24f0a6b8553 |
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| Source note | uspto-grants-2014_12 |
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