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CAS No. : | 138108-72-2 | MDL No. : | MFCD03094725 |
Formula : | C10H19NO3 | Boiling Point : | - |
Linear Structure Formula : | - | InChI Key : | HKIGXXRMJFUUKV-MRVPVSSYSA-N |
M.W : | 201.26 | Pubchem ID : | 1514340 |
Synonyms : |
|
Chemical Name : | (R)-tert-Butyl 3-(hydroxymethyl)pyrrolidine-1-carboxylate |
Signal Word: | Warning | Class: | N/A |
Precautionary Statements: | P261-P305+P351+P338 | UN#: | N/A |
Hazard Statements: | H315-H319-H335 | Packing Group: | N/A |
GHS Pictogram: |
* All experimental methods are cited from the reference, please refer to the original source for details. We do not guarantee the accuracy of the content in the reference.
Yield | Reaction Conditions | Operation in experiment |
---|---|---|
73% | Resolution of racemate; | Racemic l-t-butoxycarbonylpyrrolidine-3-methanol (15 g,74.53 mmol) was chromatographed on a chiral column[ChiralPak AD 8 X 25 cm; 2.5% of (6% MeOH/94% EtOH); 400mL/min; UV: 210 nm] to give l-t-butoxycarbonylpyrrolidine-3-methanol:Isomer I (Rt: 8.81 min, ChiralPak AD 4.6 X 250 mm; 1.0mL/min; UV: 210 nm) (6.35 g, 42%, 94% ee) andIsomer II (Rt: 9.68 min)' (6.43 g, 43%, 90% ee) .Isomer I: FIA-MS, m/e: 202.2 (rrH-1) .Isomer II: FIA-MS, m/e: 202.2 (m+1). |
Yield | Reaction Conditions | Operation in experiment |
---|---|---|
<strong>[145742-50-3]4-amino-5-chloro-2-methoxybenzaldehyde</strong> (3a) (462 mg, 2.49 mmol) was dissolved in 49 toluene (15 ml), 50 triethylamine (630 mg, 6.22 mmol) was added thereto, and then 51 triphosgene (554 mg, 1.87 mmol) was added under N2 protection, followed by a reaction at 120C for 1 hour. After cooling to room temperature, Reaction Solution 1 was obtained. 44 Tert-butyl (3R)-3-(hydroxymethyl)pyrrolidine-1-carboxylate (4B) (500 mg, 2.49 mmol) was dissolved in 13 tetrahydrofuran (15 ml), to which triethylamine (630 mg, 6.22 mmol) and then Reaction Solution 1 were added, followed by a reaction at 85C for 3 hours. The reaction solution was cooled to room temperature, and water (50 ml) was added thereto, which was extracted with ethyl acetate (100 mL×2). The organic phases were combined, dried over anhydrous sodium sulfate, filtered, and the filtrate was concentrated under reduced pressure, to obtain 46 tert-butyl (3R)-3-[(2-chloro-4-formyl-5-methoxy-phenyl)carbamoyloxymethyl] pyrrolidine-1-carboxylate (4C) as a brown liquid, which was directly used in the next step without purification. LCMS m/z =451.4[M+39]. |
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