HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 472986Generated: October 26, 2026
Bis(trimethylsilyl)carbodiimide → HCID 178511854, compound
https://huagongshe.com/reaction/472986
Participants
| Role | Name | HCID | Charge |
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| Reactant | Bis(trimethylsilyl)carbodiimide | HCID 70473 | — |
| Reactant | 6'-bromo-5,6,8,9-tetrahydrospiro[benzo[7]annulene-7,2'-inden]-1'(3'H)-one | HCID 58197349 | — |
| Catalyst | Titanium Tetrachloride | HCID 24193 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | HCID 178511854 | HCID 178511854 | 92.8% |
Reaction Steps
To a solution of 6′-bromo-5,6,8,9-tetrahydrospiro[benzo[7]annulene-7,2′-inden]-1′(3′H)-one (20 mg, 0.059 mmol) in DCM (2 mL) was added TiCl4 (44.7 mg, 0.235 mmol) dropwise, the mixture was stirred at 50° C. at Ar2 under microwave for 20 minutes, N,N′-methanediylidenebis(1,1,1-trimethylsilanamine) (43.8 mg, 0.235 mmol) was added dropwise. The mixture was stirred at 60° C. at Ar2 under microwave for 10 minutes and repeated the same operation for one time and then poured into ice-water (10 mL). The aqueous layer was extracted with CH2Cl2, which was combined with the organic layer. The organic layer was dried and concentrated to give crude (Z)—N-(5′-bromo-5,6,8,9-tetrahydrospiro[benzo[7]annulene-7,2′-indene]-3′(1′H)-ylidene)cyanamide (20 mg, 4%).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08633212B2 |
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| Source dataset | uspto-grants-2014_01 |
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| ORD ID | ord-261f927d238240a8b01bdfbd5ae2310b |
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| Source note | uspto-grants-2014_01 |
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