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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2117005Generated: October 31, 2026

Diazomethane → HCID 86585257, compound

https://huagongshe.com/reaction/2117005

Reaction equation

Participants

RoleNameHCIDCharge
ReactantDiazomethaneHCID 9550—
ReactantIsobutyl chloroformateHCID 62365—
ReactantDiisopropylethylamineHCID 81531—
ReactantBOC-TYR(BOC)-OHHCID 7010630—
SolventDiethyl EtherHCID 3283—
SolventTetrahydrofuranHCID 8028—
ProductHCID 86585257HCID 86585257—

Reaction Steps

N,O-Bis-Boc-(S)-tyrosine (6.00 g, 15.73 mmol) was dissolved in THF (40 mL), the solution stirred under an argon atmosphere and cooled in an ice bath. Isobutyl chloroformate (3.0 6 mL, 23.59 mmol) was added followed by DIEA (8.22 mL, 47.19 mmol). Additional isobutyl chloroformate (1 mL) was added after 1.5 and 2.5 h. To the cold suspension was then added a ca 0.6M Et2O solution of diazomethane (80 mL) by portions. After 15 min. of stirring, nitrogen was diffused in the solution for 0.5 hr. The solvent was evaporated, the residue taken into EtOAc (75 ml) and the solution washed with 0.5M aqueous citric acid (2×50 mL), 5% aqueous sodium bicarbonate (2×50 mL) and brine (50 mL). After drying (MgSO4) and evaporation of the solvent under reduced pressure, the residue was purified by flash chromatography (20% EtOAc/hexane) to give the title compound (5.52 g) of a yellowish solid.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07439258B2
Source datasetuspto-grants-2008_10
ORD IDord-2d2e68a0c31f4d37b22059221231138f
Source noteuspto-grants-2008_10