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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 547118Generated: November 1, 2026

Trimethylsilyldiazomethane → HCID 56930596, compound

https://huagongshe.com/reaction/547118

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTrimethylsilyldiazomethaneHCID 167693—
ReactantPotassium bisulfateHCID 516920—
ReactantHCID 67065186HCID 67065186—
SolventDiethyl EtherHCID 3283—
ProductHCID 56930596HCID 5693059697.2%

Reaction Steps

A 0.5 N potassium bisulfate aqueous solution (7.9 mL) was added to a suspension of dicyclohexylammonium (R)-t-butoxycarbonylamino-(4-chloro-phenyl)acetate (605.6 mg, 1.30 mmol) in ether (16 mL), and the mixture was stirred for 10 minutes. Then, the aqueous layer was extracted with ether. The organic layer was washed with water and then brine, dried over anhydrous magnesium sulfate and then concentrated under reduced pressure. The resulting residue was dissolved in benzene (3.6 mL) and methanol (1.8 mL). A solution of trimethylsilyldiazomethane in ether (2 M, 0.71 mL, 1.43 mmol) was added dropwise under cooling with ice, and then the mixture was stirred for 10 minutes. The reaction mixture was concentrated under reduced pressure. The residue was purified by silica gel chromatography (hexane/ethyl acetate=4/1) to give the title compound (378.9 mg, 97%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07935688B2
Source datasetuspto-grants-2011_05
ORD IDord-898e1e88e5d545a1a774a3f335850c3c
Source noteuspto-grants-2011_05