HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 624955Generated: October 30, 2026
Diisopropylcarbodiimide → HCID 90203307, compound
https://huagongshe.com/reaction/624955
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Diisopropylcarbodiimide | HCID 12734 | — |
| Reactant | N-Hydroxysuccinimide | HCID 80170 | — |
| Reactant | 1-Boc-4,4-dimethyl-pyrrolidine-2-carboxylic acid | HCID 22235308 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | HCID 90203307 | HCID 90203307 | 70% |
Reaction Steps
A solution of 4,4-dimethyl-pyrrolidine-1,2-dicarboxylic acid 1-tert-butylester (2.0 g, 8.22 mmol) in THF (20 mL) was cooled to 0° C. To the cold solution was added N-hydroxysuccinimide (1.2 g, 10.4 mmol) and diisopropylcarbodiimide (1.32 g, 10.4 mmol). Cooling was removed and the mixture stirred for 3 hours at room temperature. The urea was filtered off, washed with diethylether and the filtrates were concentrated. The residue was partitioned between ethyl acetate and cold water; organic phases were washed with cold brine, combined, dried with MgSO4, filtered and concentrated in vacuo. The residue was purified by flash chromatography (silica, heptane/ethyl acetate 9:1) to give the title compound (1.95 g, 70%) as colorless oil; MS (ESI) 341.1 [MH+].
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US09303012B2 |
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| Source dataset | uspto-grants-2016_04 |
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| ORD ID | ord-c88c26994e13486b80793f3ccaadd2f6 |
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| Source note | uspto-grants-2016_04 |
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