Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2054006Generated: October 31, 2026

Triethylamine → HCID 86620557, compound

https://huagongshe.com/reaction/2054006

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTriethylamineHCID 8471—
ReactantDiazomethaneHCID 9550—
ReactantIsobutyl chloroformateHCID 62365—
ReactantHCID 7017888HCID 7017888—
SolventAcetic AcidHCID 176—
SolventTetrahydrofuranHCID 8028—
Solventtert-Butyl methyl etherHCID 15413—
ProductHCID 86620557HCID 86620557—

Reaction Steps

5.0 g (14.9 mmol) of 1-benzyl tert-butoxycarbonyl-(S)-glutamate is placed in 75 mL of tetrahydrofuran while cooling with ice, combined with 2.1 mL (16.5 mmol) of isobutylchloroformate and 2.5 mL (18 mmol) of triethylamine, and stirred for 60 minutes. Then 30 mL, (20 mmol) of diazomethane (0.7 molar in diethyl ether) and 200 mL of tert-butylmethylether are added and the mixture is stirred overnight at ambient temperature. After the addition of 1 mL glacial acetic acid, the phases are separated, and the organic phase is dried and concentrated by evaporation. The residue is chromatographed on silica gel, eluting with dichloromethane/ethyl acetate (0%-20%). Yield: 2.2 g (41%); Rf value: 0.42 (silica gel: petroleum ether/ethyl acetate=6:4); C18H23N3O5 (361.40); mass spectrum: (M+H)+=362

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07326791B2
Source datasetuspto-grants-2008_02
ORD IDord-1b9be11135ed43a39533553185fc431e
Source noteuspto-grants-2008_02