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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 458321Generated: October 30, 2026

2,5-Difluorobenzaldehyde → HCID 69433288, compound

https://huagongshe.com/reaction/458321

Reaction equation

Participants

RoleNameHCIDCharge
Reactant2,5-DifluorobenzaldehydeHCID 137663—
ReactantHCID 11752390HCID 11752390—
ReactantHCID 69431247HCID 69431247—
ProductHCID 69433288HCID 69433288—

Reaction Steps

From (2S,4R)-2-azidomethyl-4-tritylsulfanyl-pyrrolidine-1-carboxylic acid tert-butyl ester was prepared via (2S,4R)-2-aminomethyl-4-tritylsulfanyl-pyrrolidine-1-carboxylic acid tert-butyl ester [as light brown foam, MS: 475 (MH+)] and further reaction with 2,5-difluoro benzaldehyde analogously to reductive amination gave (2S,4R)-2-[(2,5-difluoro-benzylamino)-methyl]-4-tritylsulfanyl-pyrrolidine-1-carboxylic acid tert-butyl ester as colorless oil MS: 601 (MH+) which was treated according to trityl cleavage (method 5) to give (2S,4R)-2-[(2,5-difluoro-benzylamino)-methyl]-4-mercapto-pyrrolidine-1-carboxylic acid tert-butyl ester as colorless liquid MS: 359 (MH+).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07189756B2
Source datasetuspto-grants-2007_03
ORD IDord-a12ada0f8cb849d484e3543262b09153
Source noteuspto-grants-2007_03