HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 337229Generated: October 29, 2026
Phenylacetyl chloride → HCID 64793016, compound
https://huagongshe.com/reaction/337229
Participants
| Role | Name | HCID | Charge |
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| Reactant | Phenylacetyl chloride | HCID 7679 | — |
| Reactant | Tetrahydrofuran | HCID 8028 | — |
| Reactant | 4-Aminobenzyl alcohol | HCID 69331 | — |
| Reactant | Sodium Bicarbonate | HCID 516892 | — |
| Solvent | Water | HCID 962 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | HCID 64793016 | HCID 64793016 | 57.4% |
Reaction Steps
Sodium bicarbonate (1.0 g, 12.2 mmol) was added portion-wise to a stirred solution of (4-amino-phenyl)-methanol (0.5 g, 4.06 mmol) in a 1:1 mixture of THF:H2O (16 ml) and the mixture was stirred at room temperature for 5 minutes. After this time, benzyl carbonyl chloride (0.69 g, 4.06 mmol) was added dropwise, followed by a further portion of sodium bicarbonate (0.5 g, 6.1 mmol) and stirring was continued for 1 hour. The reaction mixture was then diluted with DCM (50 ml) and washed sequentially with HCl (1M solution, 10 ml) then NaOH (1M solution, 10 ml). The organic layer was separated, dried (MgSO4), filtered and concentrated. The resulting residue was purified by flash column chromatography (elution: 50% EtOAc, 50% heptane) to give the title compound (0.6 g, 57% yield) as an off-white solid. δH (500 MHz, DMSO) 9.63 (s, 1 H) 7.01-7.39 (m, 9 H) 4.90-5.11 (m, 3 H) 4.30 (d, J=5.63 Hz, 2 H).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08889716B2 |
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| Source dataset | uspto-grants-2014_11 |
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| ORD ID | ord-16ec991b84fa40cdade2f542728c1d72 |
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| Source note | uspto-grants-2014_11 |
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