Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Triethylamine | HCID 8471 | — |
| Reactant | Ammonium Chloride | HCID 25517 | — |
| Reactant | Methanesulfonyl chloride | HCID 31297 | — |
| Reactant | 7-(Hydroxymethyl)-2-naphthalenecarboxaldehyde | HCID 18413828 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | HCID 88107267 | HCID 88107267 | — |
Reaction Steps
To a cold (0° C.) solution of the product of step 6 (430 mg, 2.31 mmol) in CH2Cl2 (5 mL) was added MsCl (318 mg, 2.7 mmol) and Et3N (559 mg, 5.5 mmol). The mixture was stirred at 0° C. for 2 h. Aqueous NH4Cl was added, and the mixture was extracted with EtOAc. The combined organic extracts were washed with brine, dried (anhyd. MgSO4) and concentrated in vacuo. The crude product was used in the next step without further purification.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US06465444B2 |
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| Source dataset | uspto-grants-2002_10 |
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| ORD ID | ord-3af8b0e1f69440b8960ebfee4bdb52c9 |
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| Source note | uspto-grants-2002_10 |
|---|