HuagongsheHuagongshe Chemistry Print Report · For research reference only
Methanol → HCID 15942620, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Methanol | HCID 887 | — |
| Reactant | Triphenylphosphine | HCID 11776 | — |
| Reactant | HCID 86609123 | HCID 86609123 | — |
| Solvent | Water | HCID 962 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Solvent | Ammonium Hydroxide | HCID 14923 | — |
| Product | HCID 15942620 | HCID 15942620 | — |
Reaction Steps
To a solution of (R)-2-azidomethyl-8-(2-chloro-phenyl)-6-fluoro-chroman (210 mg, 0.67 mmol) in tetrahydrofuran (10 mL) and water (0.5 mL) was added triphenylphosphine (0.26 g, 10 mmol) and the reaction mixture stirred at room temperature for 24 hours. The solvent was removed under vacuum to form a colorless oil. Chromatography with 0–5% methanol in methylene chloride plus 1% NH4OH afforded {[(R)-8-(2-chlorophenyl)-6-fluoro-2H-chromen-2-yl]methyl}amine as a colorless oil. The colorless oil was dissolved in ethyl acetate and made into its hydrochloride salt (56 mg, 25%) as a beige solid using excess ethereal hydrochloric acid, mp 145–147° C.; [α]D25=+256.01° (c=5.3 mg/0.7 mL MeOH).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US07365095B2 |
| Source dataset | uspto-grants-2008_04 |
| ORD ID | ord-6dba26affedf4d5abbd0487e5acd6687 |
| Source note | uspto-grants-2008_04 |