HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 547118Generated: November 1, 2026
Trimethylsilyldiazomethane → HCID 56930596, compound
https://huagongshe.com/reaction/547118
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Trimethylsilyldiazomethane | HCID 167693 | — |
| Reactant | Potassium bisulfate | HCID 516920 | — |
| Reactant | HCID 67065186 | HCID 67065186 | — |
| Solvent | Diethyl Ether | HCID 3283 | — |
| Product | HCID 56930596 | HCID 56930596 | 97.2% |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07935688B2 |
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| Source dataset | uspto-grants-2011_05 |
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| ORD ID | ord-898e1e88e5d545a1a774a3f335850c3c |
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| Source note | uspto-grants-2011_05 |
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