HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2096640Generated: October 31, 2026
Bis(trimethylsilyl)carbodiimide → N-(6-(phenylethynyl)-2',4',5',6'-tetrahydrospiro[chroman-2,3'-pyran]-4-ylidene)cyanamide
https://huagongshe.com/reaction/2096640
Participants
| Role | Name | HCID | Charge |
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| Reactant | Bis(trimethylsilyl)carbodiimide | HCID 70473 | — |
| Reactant | 6-(Phenylethynyl)-2',4',5',6'-tetrahydrospiro[chroman-2,3'-pyran]-4-one | HCID 58424694 | — |
| Catalyst | Titanium Tetrachloride | HCID 24193 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | N-(6-(phenylethynyl)-2',4',5',6'-tetrahydrospiro[chroman-2,3'-pyran]-4-ylidene)cyanamide | HCID 58424611 | 121.2% |
Reaction Steps
To a solution of 6-(phenylethynyl)-2′,4′,5′,6′-tetrahydrospiro[chroman-2,3′-pyran]-4-one (86 mg, 0.27 mmol) in anhydrous DCM (10 mL) under N2 atmosphere was added 1 M TiCl4 (in DCM, 0.54 mL, 0.54 mmol) dropwise within 15 min at room temperature. It was stirred another 1 h after the addition. To this mixture was added Bis-trimethylsilylcarbodiimide (0.16 mL, 0.427 mmol) dropwise. The resulting mixture was stirred 80 h. The reaction mixture was quenched with ice-water (15 g), and stirred for 30 min, then it was transferred to a separating funnel, the separated aqueous phase was extracted 2 times with DCM. The combined organic phases were dried over anhydrous Na2SO4, and filtered, and concentrated to give 112 mg the crude desired product as light yellow solid, which was used for next step without further purification. MS ESI +ve m/z 343 (M+H)+.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08450308B2 |
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| Source dataset | uspto-grants-2013_05 |
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| ORD ID | ord-b80e9023ce7c494fb7cd1d1f7db1bdeb |
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| Source note | uspto-grants-2013_05 |
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