HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 921058Generated: November 3, 2026
Benzoyl chloride → HCID 118353317, compound
https://huagongshe.com/reaction/921058
Participants
| Role | Name | HCID | Charge |
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| Reactant | Benzoyl chloride | HCID 7412 | — |
| Reactant | Triethylamine | HCID 8471 | — |
| Reactant | 2-(4-Bromophenyl)ethanol | HCID 72851 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | HCID 118353317 | HCID 118353317 | 99% |
Reaction Steps
To a mixture of 2-(4-bromophenyl)ethanol (1.00 g, 4.97 mmol, 1.00 equiv) and Et3N (0.763 ml, 0.554 g, 5.47 mmol, 1.10 equiv) in a round-bottom flask in THF (20 ml) was added benzoyl chloride (0.589 mL, 0.713 g, 5.07 mmol, 1.02 equiv). The reaction mixture was stirring for 4 h at 23 ° C. and concentrated in vacuo. The residue was purified by chromatography on silica gel eluting with hexanes/EtOAc 1:1 (v/v) to afford 1.50 g of the title compound as a colorless solid (99%). Rf=0.7 (hexanes/EtOAc 1:1 (v/v)). NMR Spectroscopy: 1H NMR (500 MHz, CDCl3, 23 ° C., δ): 8.00 (d, J=7.2 Hz, 1H), 7.58-7.54 (m, 1H), 7.45-7.42 (m, 4H), 7.16 (d, J=8.4 Hz, 2H), 4.51 (t, J=6.4 Hz, 2H), 3.04 (t, J=6.4 Hz, 2H). 13C NMR (125 MHz, CDCl3, 23 ° C., δ): 166.6, 137.1, 133.1, 131.8, 130.8, 130.3, 129.7, 128.5, 120.6, 65.2, 34.8.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US09273083B2 |
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| Source dataset | uspto-grants-2016_03 |
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| ORD ID | ord-8da636bde9f049afb3bdfb855badf4c4 |
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| Source note | uspto-grants-2016_03 |
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