HuagongsheHuagongshe Chemistry Print Report · For research reference only
Methyl iodide → HCID 21940430, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Methyl iodide | HCID 6328 | — |
| Reactant | Ethyl Acetate | HCID 8857 | — |
| Reactant | Sodium hydride | HCID 24758 | — |
| Reactant | 2-(Boc-amino)-1,2,3,4-tetrahydronaphthalene-2-carboxylic acid | HCID 2733177 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Product | HCID 21940430 | HCID 21940430 | — |
Reaction Steps
To 2-tert-butoxycarbonylamino-1,2,3,4-tetrahydro-naphthalene-2-carboxylic acid (291 mg, 1.0 mmol) in DMF (2.0 mL) was added MeI (710 mg, 5.0 mmol) and NaH (50%, 250 mg, 5.0 mmol) at 0° C. Ethyl acetate (50 mL) was added after 3 days and the mixture was washed with water (3×15 mL). The material (380 mg) was taken up in methanol (5.0 mL) and water (3.0 mL) and NaOH (10 M, 3.0 mL) was added. After 2 days, 10% HCl was added to adjust the pH˜2 and the mixture was extracted with ethyl acetate (3×20 mL). The organic layers were concentrated in vacuo to provide the titled acid.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US07115767B2 |
| Source dataset | uspto-grants-2006_10 |
| ORD ID | ord-1c95195afe6a497db876ec98accdeaf4 |
| Source note | uspto-grants-2006_10 |