Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Methanol | HCID 887 | — |
| Reactant | Trimethylsilyldiazomethane | HCID 167693 | — |
| Reactant | 2-Iodophenylacetic acid | HCID 2780090 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | Methyl 2-(2-iodophenyl)acetate | HCID 640185 | 100% |
Reaction Steps
Trimethylsilyl diazomethane (15.3 ml, 30.6 mmol, 2.0 M in diethyl ether) was added dropwise to a stirred, cooled 0° C. solution of (2-iodophenyl)acetic acid (4.0 g, 15.3 mmol) and MeOH (10 ml) in CH2Cl2 (50 ml) and the solution was stirred at 0° C. for 1 hour. The yellow solution was purged with nitrogen for 10 minutes. The solvent removed in vacuo and the residue was azeotroped with THF (3×25 ml) to afford 4.2 g, 100% of 23-1 as a yellow oil.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08119681B2 |
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| Source dataset | uspto-grants-2012_02 |
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| ORD ID | ord-d860ee30052a4724a85288e43eea1749 |
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| Source note | uspto-grants-2012_02 |
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