HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1594497Generated: October 30, 2026
HCID 69497460, compound → HCID 13040227, compound
https://huagongshe.com/reaction/1594497
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | HCID 69497460 | HCID 69497460 | — |
| Reactant | HCID 69497549 | HCID 69497549 | — |
| Solvent | Acetonitrile | HCID 6342 | — |
| Product | HCID 13040227 | HCID 13040227 | — |
| Product | HCID 86760584 | HCID 86760584 | — |
Reaction Steps
A more powerful 100 W high pressure mercury arc lamp was initially used for the irradiation of α-phenyl-2-nitrobenzyltrichloroacetate (33) and α-(3-methoxyphenyl)-2-nitrobenzyl-trichloroacetate (35) at 365 nm (Scheme 3). The rate of photoconversion was monitored by HPLC, TLC and UV. Depending on the concentration of solution (0.002-2% in acetonitrile) and the length of light path used (1-10 mm) the rate of photoconversion varied between 20% and 90% for a 5 min irradiation. The products of photolysis, 2-nitrosobenzophenone (47) and 3′-methoxy-2-nitrosobenzophenone (48), were isolated by HPLC and showed by mass spectroscopy to be the same as those isolated previously during irradiations at 254 and 350 nm in the photoreactor described above. Secondary photoproducts were not observed under the conditions of relatively weak irradiation used in the photoreactor (4 W lamp), but were observed when the 100 W high pressure Hg arc lamp was used for extended time.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07301049B2 |
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| Source dataset | uspto-grants-2007_11 |
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| ORD ID | ord-02cb040a8fd2480d9cf07dd2380f522d |
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| Source note | uspto-grants-2007_11 |
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