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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1442959Generated: November 1, 2026

Sodium Hydroxide → HCID 59166754, compound

https://huagongshe.com/reaction/1442959

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSodium HydroxideHCID 14798—
Reactant4-BromothiophenolHCID 66049—
ReactantSodium ethoxideHCID 2723922—
Reactant1-tert-Butyl 2-methyl (2S,4R)-4-[(4-methylbenzene-1-sulfonyl)oxy]pyrrolidine-1,2-dicarboxylateHCID 13425772—
SolventEthanolHCID 702—
ProductHCID 59166754HCID 5916675440%

Reaction Steps

Sodium ethoxide (112 mg, 1.65 mmol) was added slowly to a stirred solution of 4-bromothiophenol (302 mg, 1.65 mmol) in EtOH (6 ml) at room temperature under a nitrogen atmosphere. A solution of (2S,4R)-4-(toluene-4-sulfonyloxy)-pyrrolidine-1,2-dicarboxylic acid 1-tert-butyl ester 2-methyl ester (CAS Reg. No. 88043-21-4) (300 mg, 0.75 mmol) in 1 ml EtOH was added after 30 minutes and the solution was stirred for 48 h. The reaction mixture was poured into 0.5M NaOH (50 ml) and extracted with CH2Cl2 (2×50 ml). The combined organics were dried (magnesium sulphate) and concentrated under vacuum. Flash column chromatography yielded the product as a pink solid (120 mg, 40%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07659305B2
Source datasetuspto-grants-2010_02
ORD IDord-6e2b32262c3e43a0b45f9761aa6fbe3f
Source noteuspto-grants-2010_02