HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2242204Generated: November 2, 2026
Phenyl chloroformate → HCID 11645712, compound
https://huagongshe.com/reaction/2242204
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Phenyl chloroformate | HCID 15891 | — |
| Reactant | Diisopropylethylamine | HCID 81531 | — |
| Reactant | HCID 69241294 | HCID 69241294 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | HCID 11645712 | HCID 11645712 | — |
Reaction Steps
To a solution of Example 17D (32 mg, 0.1 mmol) in anhydrous THF (5 mL) was added N,N-diisopropylethylamine (0.035 mL, 0.2 mmol), followed by phenyl chloroformate (17.22 mg, 0.11 mmol). The mixture was stirred for 8 hours at room temperature and concentrated under reduced pressure. The residue was taken up in anhydrous dichloromethane (3 mL) and trifluoracetic acid (0.075 mL) in dichloromethane (0.075 mL) were added. The mixture was stirred for 5 hours at room temperature, concentrated under reduced pressure and purified using RP-HPLC to provide the titled compound. MS (ESI) m/e 336 (M+H)+; 1H NMR (400 MHz, CD3OD) δ ppm 1.77 (m, 1 H) 2.69 (m, 2 H) 3.07 (m, 1 H) 3.17 (m, 2 H) 3.25 (m, 1 H) 3.52 (m, 2 H) 3.75 (m, 1 H) 3.88 (m, 1 H) 4.52 (m, 1 H) 4.66 (m, 2 H) 7.10 (d, 2 H) 7.21 (t, 1 H) 7.37 (t, 2 H).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07671076B2 |
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| Source dataset | uspto-grants-2010_03 |
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| ORD ID | ord-9cb50a85541c44219c7479e1eff7d3f2 |
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| Source note | uspto-grants-2010_03 |
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