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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1007703Generated: October 29, 2026

Diazomethane → HCID 86585257, compound

https://huagongshe.com/reaction/1007703

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 chloroform ate (3.06 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 numberUS06794404B2
Source datasetuspto-grants-2004_09
ORD IDord-0503d757caf949cbb01ee5d26a9f1248
Source noteuspto-grants-2004_09