Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1492818Generated: October 30, 2026

Lithium diisopropylamide → (2R,4S)-N-allyloxycarbonyl-2-[(5S)-5-hydroxymethyl-2-oxopyrrolidin-3-ylmethyl]-4-tritylthiopyrrolidine

https://huagongshe.com/reaction/1492818

Reaction equation

Participants

RoleNameHCIDCharge
ReactantLithium diisopropylamideHCID 2724682—
ReactantN-tert-butyldimethylsilyl-5-tert-butyldimethylsiloxymethyl-2-oxopyrrolidineHCID 57036326—
Reactant(2S,4S)-N-allyloxycarbonyl-2-iodomethyl-4-tritylthiopyrrolidineHCID 57112975—
Product(2R,4S)-N-allyloxycarbonyl-2-[(5S)-5-hydroxymethyl-2-oxopyrrolidin-3-ylmethyl]-4-tritylthiopyrrolidineHCID 5718986821%

Reaction Steps

The same procedure as in Reference Example 22-1 was carried out by using N-tert-butyldimethylsilyl-5-tert-butyldimethylsiloxymethyl-2-oxopyrrolidine (10.67 g, 31.6 mmol), lithium diisopropylamide (2.1M tetrahydrofuran solution, 15.1 ml, 31.6 mmol) and (2S,4S)-N-allyloxycarbonyl-2-iodomethyl-4-tritylthiopyrrolidine (10 g, 17.6 mmol) to obtain (2R,4S)-N-allyloxycarbonyl-2-[(5S)-5-hydroxymethyl-2-oxopyrrolidin-3-ylmethyl]-4-tritylthiopyrrolidine (2 g, yield: 21%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05374720
Source datasetuspto-grants-1994_12
ORD IDord-ff67efe4b82f4f33816effd65cff8a64
Source noteuspto-grants-1994_12