HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2112018Generated: October 25, 2026
Hydrochloric Acid → 2-[(4{3-[4-(Benzyloxy)phenoxy]propyl}phenoxy)methyl]-benzoic acid
https://huagongshe.com/reaction/2112018
Participants
| Role | Name | HCID | Charge |
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| Reactant | Hydrochloric Acid | HCID 313 | — |
| Reactant | Lithium Hydroxide | HCID 3939 | — |
| Reactant | Methyl 2-[(4-{3-[4-(benzyloxy)phenoxy]propyl}phenoxy)methyl]benzoate | HCID 68869717 | — |
| Solvent | Oxolane--water (1/1) | HCID 21881883 | — |
| Product | 2-[(4{3-[4-(Benzyloxy)phenoxy]propyl}phenoxy)methyl]-benzoic acid | HCID 10412337 | 4.4% |
Reaction Steps
Methyl 2-[(4-{3-[4-(benzyloxy)phenoxy]propyl}phenoxy)methyl]benzoate (0.047 g, 0.097 mmol) was dissolved in a mixture of THF/water (7/1, 2 ml) and lithium hydroxide (9.3 mg, 0.39 mmol) was added. The reaction was performed in a single node microwave oven (7 min, 150° C.). The reaction mixture was acidified (HCl, 1 M, 1 ml) and the water phase was washed with two portions of EtOAc (2×5 ml). The organic phases were combined, dried (MgSO4) and the solvent was removed by evaporation. The crude product was purified by preparative HPLC (started with acetonitrile/buffer 60/40 and then the acetonitrile concentration was increased to 100%, the buffer was a mixture of acetonitrile/water 10/90 and ammonium acetate (0.1 M, column KR-100-7-C8, 50 mm×250 mm, flow 40 ml/min)). The product containing fractions were pooled and the acetonitrile was removed by evaporation. EtOAc (10 ml) was added and the organic phase was washed with two portions of brine and dried (MgSO4). Removing the solvent by evaporation gave 2 mg of 2-[(4{3-[4-(benzyloxy)phenoxy]propyl}phenoxy)methyl]-benzoic acid (yield 4.4%).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07521461B2 |
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| Source dataset | uspto-grants-2009_04 |
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| ORD ID | ord-83b71f0b6f9e45088ae3dc02e782bc29 |
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| Source note | uspto-grants-2009_04 |
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