Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 234490Generated: October 25, 2026

Benzyl Bromide → Phenylmethyl 6-[[(1,1-dimethylethoxy)carbonyl]amino]hexanoate

https://huagongshe.com/reaction/234490

Reaction equation

Participants

RoleNameHCIDCharge
ReactantBenzyl BromideHCID 7498—
Reactant1,8-Diazabicyclo(5.4.0)undec-7-eneHCID 81184—
Reactant6-((tert-Butoxycarbonyl)amino)hexanoic acidHCID 637602—
SolventDichloromethaneHCID 6344—
ProductPhenylmethyl 6-[[(1,1-dimethylethoxy)carbonyl]amino]hexanoateHCID 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

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05594023
Source datasetuspto-grants-1997_01
ORD IDord-f9b768c700394298bbbed1554bf678e4
Source noteuspto-grants-1997_01