HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2071112Generated: November 1, 2026
Sodium cyanoborohydride → (R)-benzyl 2-(4-methyloxazol-2-yl)pyrrolidine-1-carboxylate
https://huagongshe.com/reaction/2071112
Participants
| Role | Name | HCID | Charge |
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| Reactant | Sodium cyanoborohydride | HCID 5003444 | — |
| Reactant | (R)-benzyl 2-(4-(hydroxymethyl)oxazol-2-yl)pyrrolidine-1-carboxylate | HCID 86647435 | — |
| Catalyst | Methyltriphenoxyphosphonium iodide | HCID 2735090 | — |
| Solvent | Hexamethylphosphoramide | HCID 12679 | — |
| Product | (R)-benzyl 2-(4-methyloxazol-2-yl)pyrrolidine-1-carboxylate | HCID 86647436 | 17.3% |
Reaction Steps
To a solution of (R)-benzyl 2-(4-(hydroxymethyl)oxazol-2-yl)pyrrolidine-1-carboxylate (1.1 g, 3.64 mmoles) in HMPA (18 mL), was added methyltriphenoxyphosphonium iodide (3.29 g, 7.28 mmoles) and stirred for 30 min. Then NaCNBH3 was added and the reaction was heated at 50° C. for 3 h and poured into 100 mL of ice-cold water and extracted with ether (2×100 mL). The organic layer was dried on Na2SO4, concentrated, and chromatographed on silica gel (50% ethyl acetate/50% hexanes) to yield 180 mg of (R)-benzyl 2-(4-methyloxazol-2-yl)pyrrolidine-1-carboxylate.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08299267B2 |
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| Source dataset | uspto-grants-2012_10 |
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| ORD ID | ord-d52c605f8578400da0032e7ef615ac0a |
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| Source note | uspto-grants-2012_10 |
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