HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 412488Generated: October 28, 2026
Ammonium Chloride → HCID 22977309, compound
https://huagongshe.com/reaction/412488
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Ammonium Chloride | HCID 25517 | — |
| Reactant | (2R)-Oxiran-2-ylmethyl butanoate | HCID 2724536 | — |
| Reactant | Lithium Hexamethyldisilazide | HCID 2733832 | — |
| Reactant | HCID 22245080 | HCID 22245080 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | HCID 22977309 | HCID 22977309 | — |
Reaction Steps
1 M Lithium bis(trimethylsilyl)amide in tetrahydrofuran (1.1 mL, 1.1 mmol) was added dropwise with stirring at −78° C. to 5-benzyloxycarbonylamino-1-tritylindazole (0.510 g, 1 mmol) in tetrahydrofuran (10 mL) under nitrogen atmosphere. The mixture was stirred at −78° C. for 1.5 h. (R)-Glycidyl butyrate (0.160 mL, 1.2 mmol) was added dropwise with stirring. The mixture was allowed to warm to r.t. overnight. Saturated aq. NH4Cl (10 mL) was added, and the mixture was extracted with EtOAc (2×20 mL). The combined organic layers were washed with water (10 mL), brine (10 mL), and dried (MgSO4). Solvent was evaporated to 3 mL, and the residue was triturated with hexanes (50 mL). White crystalline product was filtered off, washed with hexanes, and dried in vacuo. Yield 0.440 g (93%). MS (m/z): 232.1 [M-Trt]−. 1H NMR.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US06562844B2 |
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| Source dataset | uspto-grants-2003_05 |
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| ORD ID | ord-73abbc97f8584cab9ae8e6c2d4faca50 |
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| Source note | uspto-grants-2003_05 |
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