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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2267466Generated: October 30, 2026

Triethylamine → (S)-tert-Butyl 2-((benzo[b]thiophen-5-yloxy)methyl)pyrrolidine-1-carboxylate

https://huagongshe.com/reaction/2267466

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTriethylamineHCID 8471—
ReactantTriphenylphosphineHCID 11776—
Reactant(S)-(-)-N-Boc-prolinolHCID 643448—
ReactantDiisopropyl azodicarboxylateHCID 5363146—
ReactantBenzo[b]thiophen-5-olHCID 12203499—
SolventDichloromethaneHCID 6344—
Product(S)-tert-Butyl 2-((benzo[b]thiophen-5-yloxy)methyl)pyrrolidine-1-carboxylateHCID 86614160—

Reaction Steps

Polystyrene supported triphenylphosphine (2.9 mmol/g, 1.70 g, 4.95 mmol) was treated with diisopropylazodicarboxylate (0.779 mL, 3.96 mmol) at 0° C. in anhydrous dichloromethane. A mixture of (S)-tert-butyl 2-(hydroxymethyl)pyrrolidine-1-carboxylate (0.5 g, 3.3 mmol), benzo[b]thiophen-5-ol (0.5 g, 3.3 mmol) and triethylamine (0.689 mL, 4.95 mmol) in dichloromethane (5 mL) was then added to the reaction. The mixture was then allowed to warm up to room temperature and stirred overnight. The reaction was then filtered off and the filtrate purified by column chromatography on silica gel using a gradient of 15 to 50% ethyl acetate in hexanes to obtain a clear oil that solidied into an off-white solid on standing. Yield=0.48 g. MS (M+H)+ 334.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07858785B2
Source datasetuspto-grants-2010_12
ORD IDord-5bf7a0b128294b4cbf67bf6e9b5a631b
Source noteuspto-grants-2010_12