HuagongsheHuagongshe Chemistry Print Report · For research reference only
Bis(trimethylsilyl)carbodiimide → HCID 178511855, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Bis(trimethylsilyl)carbodiimide | HCID 70473 | — |
| Reactant | HCID 58197381 | HCID 58197381 | — |
| Catalyst | Titanium Tetrachloride | HCID 24193 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | HCID 178511855 | HCID 178511855 | 113.4% |
Reaction Steps
To a solution of 6-bromo-5′,6′-difluoro-3′,4′-dihydro-1′H-spiro[indene-2,2′-naphthalen]-1(3H)-one (150 mg, 0.41 mmol) in dried CH2Cl2 (1 mL) was added TiCl4 (1 M solution in DCM, 0.1.24 mmol) dropwise within 15 minutes, and stirred for 1 h. Then to this mixture was added bis-trimethlysilylcarbodiimide (234 mg, 1.24 mmol) dropwise. The resulting mixture was stirred overnight. The reaction mixture was poured into ice-water, extracted with CH2Cl2. The combined organic layer was washed with brine, dried over Na2SO4, filtered and concentrated to give (Z)—N-(5-bromo-5′,6′-difluoro-3′,4′-dihydro-1′H-spiro[indene-2,2′-naphthalene]-3(1H)-ylidene)cyanamide (180 mg, crude), which was used for the next step without further purification.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US09212153B2 |
| Source dataset | uspto-grants-2015_12 |
| ORD ID | ord-b17b991016194eb4b697676852121a08 |
| Source note | uspto-grants-2015_12 |