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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

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSodium cyanoborohydrideHCID 5003444—
Reactant(R)-benzyl 2-(4-(hydroxymethyl)oxazol-2-yl)pyrrolidine-1-carboxylateHCID 86647435—
CatalystMethyltriphenoxyphosphonium iodideHCID 2735090—
SolventHexamethylphosphoramideHCID 12679—
Product(R)-benzyl 2-(4-methyloxazol-2-yl)pyrrolidine-1-carboxylateHCID 8664743617.3%

Reaction Conditions

Temperature50 °C

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

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08299267B2
Source datasetuspto-grants-2012_10
ORD IDord-d52c605f8578400da0032e7ef615ac0a
Source noteuspto-grants-2012_10