HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1532846Generated: October 30, 2026
Potassium Carbonate → 4-Thioacetoxymethyl-2-phenylbenzoic acid methyl ester
https://huagongshe.com/reaction/1532846
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Potassium Carbonate | HCID 11430 | — |
| Reactant | Triphenylphosphine | HCID 11776 | — |
| Reactant | 2-Thiopheneacetic acid | HCID 15970 | — |
| Reactant | Diethyl azodicarboxylate | HCID 5462977 | — |
| Reactant | Methyl 4-hydroxymethyl-2-phenylbenzoate | HCID 10824066 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | 4-Thioacetoxymethyl-2-phenylbenzoic acid methyl ester | HCID 86586789 | — |
Reaction Steps
To triphenylphosphine (1.2 equivalents) in THF at −78° C. is added diethylazodicarboxylate (1.2 equivalents) in THF. After 10 min thiolacetic acid (1.3 equivalents) in THF is added followed by the resultant compound from Example 16B (1. equivalent) in THF. The reaction is stirred at −78° C. for 1 h and then at ambient temperature until it is judged to be complete by TLC analysis. The mixture is evaporated and the residue is taken up in methanol and is treated with K2CO3 (2 equivalents). When the reaction is judged to be complete by TLC analysis, the solvent is evaporated and the residue is chromatographed on silica gel to afford the title product.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US06204293B1 |
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| Source dataset | uspto-grants-2001_03 |
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| ORD ID | ord-adbb225228dc418ebfd97eea11a6f463 |
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| Source note | uspto-grants-2001_03 |
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