HuagongsheHuagongshe Chemistry Print Report · For research reference only
Sodium Hydroxide → 3-(Phenylmethyl)-7-oxa-3-azabicyclo[4.1.0]heptane
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Sodium Hydroxide | HCID 14798 | — |
| Reactant | N-bromobutanimide | HCID 67184 | — |
| Reactant | 1-BENZYL-1,2,3,6-TETRAHYDROPYRIDINE | HCID 6421573 | — |
| Catalyst | Trifluoroacetic acid | HCID 6422 | — |
| Solvent | Water | HCID 962 | — |
| Product | 3-(Phenylmethyl)-7-oxa-3-azabicyclo[4.1.0]heptane | HCID 6421496 | 3,337.2% |
Reaction Steps
3.36 g of 1-benzyl-1,2,3,6-tetrahydropyridine (0.19 mmol) was dissolved in 35 mL of water containing 1.5 mL of trifluoroacetic acid (0.2 mmol). To that solution 5.87 g of NBS was added in small portions. After 4 hs reaction mixture was transferred to 50 mL of 20% NaOH solution and stirred overnight. On the morning reaction mixture was extracted with dichloromethane and combined organic fractions were dried over sodium sulfate and concentrated. The residue was purified on silica gel column using hexane-ethyl acetate 3:1 as eluent. Evaporation of solvent produced 1.2 g of 3-benzyl-7-oxa-3-azabicyclo[4.1.0]heptane as colorless oil.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US09216993B2 |
| Source dataset | uspto-grants-2015_12 |
| ORD ID | ord-079f2d5f617c48c29b82e2586a37ac3c |
| Source note | uspto-grants-2015_12 |