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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1764779Generated: October 25, 2026

Methanol → Boc-Glu(OBzl)-Val-Val-OH

https://huagongshe.com/reaction/1764779

Reaction equation

Participants

RoleNameHCIDCharge
ReactantMethanolHCID 887—
ReactantTriethylamineHCID 8471—
ReactantL-Valyl-L-valineHCID 107475—
ReactantHCID 13242221HCID 13242221—
SolventDimethylformamideHCID 6228—
ProductBoc-Glu(OBzl)-Val-Val-OHHCID 131711272—

Reaction Steps

Boc-Val-Val-OH (40.5 g, 128 mmol) was treated with 1.8 l of 4N HCl in THF for 60 minutes. Evaporation to remove excess acid and solvent followed by treatment with ether provided 34.5 g of HCl.H-Val-Val-OH as a white amorphous powder. It was treated with Boc-Glu(OBzl)-OSu (55.6 g, 128 mmol) in 1 liter DMF for 24 hours in the presence of 54 ml Et3N. The reaction mixture was filtered to remove some insoluble material and the filtrate evaporated to dryness. The remaining oily residue was taken up in EtOAc (1.5 l) and washed with 5% HOAc (2×) followed by water (3×). The organic layer was dried (Na2SO4) and evaporated to dryness to give a colorless clear oil which did not crystallize. It was thus dissolved in 3.2 l of ether and treated with cyclohexylamine (CHA) (17 ml) until the pH (moist pH paper) of the mixture was 7.5. The solid salt obtained was collected and recrystallized from MeOH and ether: Yield, 58.9 g (72.7%); mp 158°-;60°; [α]D25 = -33.41° (c 1, MeOH).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04116951
Source datasetuspto-grants-1978_09
ORD IDord-70e839a5a3a941e19f9411d014dbc070
Source noteuspto-grants-1978_09