HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1994579Generated: October 30, 2026
Trimethylsilyldiazomethane → HCID 86603426, compound
https://huagongshe.com/reaction/1994579
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Trimethylsilyldiazomethane | HCID 167693 | — |
| Reactant | HCID 86603428 | HCID 86603428 | — |
| Reactant | HCID 178462185 | HCID 178462185 | — |
| Solvent | Dichloromethane methanol | HCID 21226129 | — |
| Product | HCID 86603426 | HCID 86603426 | — |
| Product | HCID 86603427 | HCID 86603427 | — |
Reaction Steps
(Trimethylsilyl)diazomethane (2M in hexanes, 459 μL, 0.918 mmol) was added dropwise to a solution of the crude benzyl [(1S,2S)-2-{[tert-butyl(dimethyl)silyl]oxy}-1-methyl-2-(1H-tetrazol-5-yl)ethyl]carbamate and benzyl [(1S,2S)-2-{[tert-butyl(dimethyl)silyl]oxy}-1-methyl-2-(2H-tetrazol-5-yl)ethyl]carbamate in CH2Cl2/MeOH (3:2, 5 mL) at room temperature under N2. After 15 min and gas evolution had ceased, the reaction mixture was concentrated in vacuo to give the crude product. This was purified by flash chromatography (Si, 12×160 mm, 0-70% EtOAc in hexanes gradient) to afford benzyl [(1S,2S)-2-{[tert-butyl(dimethyl)silyl]oxy}-1-methyl-2-(1-methyl-1H-tetrazol-5-yl)ethyl]carbamate and benzyl [(1S,2S)-2-{[tert-butyl(dimethyl)silyl]oxy}-1-methyl-2-(2-methyl-2H-tetrazol-5-yl)ethyl]carbamate, as a 2:1 mixture of regioisomers. LCMS calc.=406.2; found=406.2 (M+1)+.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07652049B2 |
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| Source dataset | uspto-grants-2010_01 |
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| ORD ID | ord-0e4c96a19e714bf7a4e47c9e409422ea |
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| Source note | uspto-grants-2010_01 |
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