HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 924761Generated: October 25, 2026
Methanol → Methyl bis(p-chlorophenyl)acetate
https://huagongshe.com/reaction/924761
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Methanol | HCID 887 | — |
| Reactant | Bis(4-chlorophenyl)acetic acid | HCID 6730 | — |
| Catalyst | Hydrochloric Acid | HCID 313 | — |
| Product | Methyl bis(p-chlorophenyl)acetate | HCID 346996 | 78% |
Reaction Steps
Bis-(4-chloro-phenyl)-acetic acid (4.33 g, 15.4 mmol) was suspended in anhydrous methanol (20 mL) and concentrated hydrochloric acid (5 drops) was added. After 1 day the reaction was quenched by the addition of saturated sodium bicarbonate solution, then the organic solvent was removed in vacuo. The residue was partitioned between ethyl acetate and 50% saturated potassium carbonate solution. The organic phase was washed with brine, dried (MgSO4), filtered and concentrated to give a residue which was purified by column chromatography (SiO2), eluting with 10% ethyl acetate/petrol, to afford the title compound as a colourless oil (3.57 g, 78%); LCMS (PS-B3) Rt 3.79 min, No Ionisation. 1H NMR (CDCl3) δ 3.74 (3H, s), 4.96 (1H, s), 7.20-7.23 (4H, m), 7.28-7.32 (4H, m).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US09283226B2 |
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| Source dataset | uspto-grants-2016_03 |
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| ORD ID | ord-83148988a6c44e259ba54bf8ba70006a |
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| Source note | uspto-grants-2016_03 |
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