HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 73269Generated: October 26, 2026
3'-Bromoacetophenone → (1-(3-Bromophenyl)ethylidene)cyanamide
https://huagongshe.com/reaction/73269
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | 3'-Bromoacetophenone | HCID 16502 | — |
| Reactant | Bis(trimethylsilyl)carbodiimide | HCID 70473 | — |
| Catalyst | Titanium Tetrachloride | HCID 24193 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | (1-(3-Bromophenyl)ethylidene)cyanamide | HCID 10966114 | 103.1% |
Reaction Steps
Following the procedure of Cuccia, S. J.; Fleming, L. B.; France, D. J. Synth. Comm. 2002, 32 (19), 3011-3018: 3-Bromoacetophenone (2.0 g, 10 mmol, 1 eq), was dissolved in 20 mL DCM. A 1.0 N solution of titanium tetrachloride in DCM (20 mL, 20 mmol, 2 eq) was added dropwise over 15 min and the resulting mixture was stirred at 25° C. for 1 h. Bis-trimethylsilylcarbodiimide (5.0 mL, 22 mmol, 2.2 eq) in 5 mL of DCM was added over 15 min and the reaction was stirred for 16 h under argon. The reaction was poured onto 200 mL of an ice/water mixture and extracted with 3×200 mL of DCM. The combined organic phase was dried over MgSO4, filtered, and concentrated to give 2.3 g (100%) of (1-(3-bromophenyl)ethylidene)cyanamide (DB1, R4=Me) as a white solid: 1H NMR (CDCl3) 8.16 (t, J=1.8 Hz, 1H), 7.94 (dd, J=1.7, 1.1 Hz, 1H), 7.76 (dd, J=1.7, 1.1 Hz, 1H), 7.38 (t, J=8.0 Hz, 1H), 2.82 (s, 3H).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08829036B2 |
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| Source dataset | uspto-grants-2014_09 |
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| ORD ID | ord-e558161646c34a6bb70f396e2175dd9a |
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| Source note | uspto-grants-2014_09 |
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