HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1264373Generated: October 25, 2026
Carbon Tetrachloride → (2S,4S)-1-tert-butyl 2-methyl 4-chloropyrrolidine-1,2-dicarboxylate
https://huagongshe.com/reaction/1264373
Participants
| Role | Name | HCID | Charge |
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| Reactant | Carbon Tetrachloride | HCID 5943 | — |
| Reactant | Dichloromethane | HCID 6344 | — |
| Reactant | Triphenylphosphine | HCID 11776 | — |
| Reactant | (2S,4R)-4-Hydroxypyrrolidine-1,2-dicarboxylic acid 1-tert-butyl ester 2-methyl ester | HCID 2734883 | — |
| Solvent | Heptane | HCID 8900 | — |
| Product | (2S,4S)-1-tert-butyl 2-methyl 4-chloropyrrolidine-1,2-dicarboxylate | HCID 11242503 | 89% |
Reaction Steps
A solution of 374 g (1.48 mol) (2S,4R)-4-Hydroxy-pyrrolidine-1,2-dicarboxylic acid 1-tert-butyl ester 2-methyl ester in 1.61 CH2Cl2 was treated with 680 g (2.6 mol) triphenylphosphine, cooled to 3-5° C. and treated in 10 min with 1.24l (12.8 mol) CCl4, after 2 h at this temperature cooling was stopped, the reaction temperature was raised to 35° C. over a period of 2 h. It was cooled down to 20° C. and stirred for further 45 min. After addition of 4l of n-heptane, the reaction was evaporated to 2.9l, cooled to 0° C., filtered, the residue was treated twice the same way, the third time by dissolving the residue again in 2 of CH2Cl2. The solvents were evaporated and filtered through silicagel with hexane/tert.-buthyl-methylether 9:1 as eluent. Evaporation of the solvents gave 347 g (89%) of (2S,4S)-4-Chloro-pyrrolidine-1,2-dicarboxylic acid 1-tert-butyl ester 2-methyl ester, MS: 246 (MH+).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US06541638B2 |
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| Source dataset | uspto-grants-2003_04 |
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| ORD ID | ord-b1712f82bd2d4ff496d5c39282b9c66a |
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| Source note | uspto-grants-2003_04 |
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