HuagongsheHuagongshe Chemistry Print Report · For research reference only
Benzyl Bromide → Phenylmethyl 6-[[(1,1-dimethylethoxy)carbonyl]amino]hexanoate
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Benzyl Bromide | HCID 7498 | — |
| Reactant | 1,8-Diazabicyclo(5.4.0)undec-7-ene | HCID 81184 | — |
| Reactant | 6-((tert-Butoxycarbonyl)amino)hexanoic acid | HCID 637602 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | Phenylmethyl 6-[[(1,1-dimethylethoxy)carbonyl]amino]hexanoate | HCID 12160267 | — |
Reaction Steps
1.94 ml of DBU and then 1.54 ml of benzyl bromide are added at RT to a solution of 3 g of 6-(tert-butoxycarbonylamino)hexanoic acid in 60 ml of DCM and the mixture is stirred for 24 hours at RT. It is concentrated under vacuum, the residue is taken up with 100 ml of water and extracted with AcOEt, the organic phase is washed with a 5% solution of potassium carbonate, with a saturated solution of NaCl and with water and dried over sodium sulfate and the solvent is evaporated off under vacuum to give 2.8 g of the expected product, which is used as such.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US05594023 |
| Source dataset | uspto-grants-1997_01 |
| ORD ID | ord-f9b768c700394298bbbed1554bf678e4 |
| Source note | uspto-grants-1997_01 |