Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Sodium Hydroxide | HCID 14798 | — |
| Reactant | HCID 67830530 | HCID 67830530 | — |
| Solvent | Methanol | HCID 887 | — |
| Product | HCID 19004389 | HCID 19004389 | 34.7% |
Reaction Steps
As in example 10, a solution of 4-[3-[4-acetyl-3-methoxy-2-propylphenoxy)propoxy]-alpha-oxobenzeneacetic acid ethyl ester (0.4 g) in methanol (30 mL) was treated with 2N sodium hydroxide (0.25 mL) was stirred at room temperature for 4 hours. Most of the solvents were removed in vacuo, water was added, then the mixture was acidified with 3N hydrochloric acid and extracted with dichloromethane-tetrahydrofuran (1:1). The dried (MgSO4) extracts were evaporated and the crude oil was purified by flash chromatography over silica gel (toluene-ethyl acetate-acetic acid; 75:25:0.5 increasing to 74:25:1) and crystallized from diethyl ether-hexane to provide 0.13 g of 4-[3-[4-acetyl-3-methoxy-2-propylphenoxy)propoxy]-alpha-oxobenzeneacetic acid, mp 94°-96° C.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US05344843 |
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| Source dataset | uspto-grants-1994_09 |
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| ORD ID | ord-9bf633d5b85d4520b5994d064b3b92e2 |
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| Source note | uspto-grants-1994_09 |
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