HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 655194Generated: October 30, 2026
(3S)-(-)-3-(tert-Butoxycarbonylamino)pyrrolidine → HCID 59211979, compound
https://huagongshe.com/reaction/655194
Participants
| Role | Name | HCID | Charge |
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| Reactant | (3S)-(-)-3-(tert-Butoxycarbonylamino)pyrrolidine | HCID 1514396 | — |
| Reactant | HCID 59212058 | HCID 59212058 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | HCID 59211979 | HCID 59211979 | — |
Reaction Steps
To a solution of 4-(3-phenoxyphenyl)morpholine-2,6-dione 26 (4.7 g, 0.0166 mol) in THF (50 mL) was added (3S)-(−)-3-(tert-butoxycarbonylamino)pyrrolidine (4.11 g, 0.0221 mol). The reaction mixture was stirred for 3 days after which time a precipitate had formed. This material was collected by filtration, then washed with ethyl acetate to give the first crop of the title compound. A further crop was obtained by evaporating the filtrate in vacuo. The resultant residue was dissolved in ethyl acetate, washed with 10% hydrochloric acid and brine, dried (Na2SO4) and concentrated in vacuo. The second crop of title compound which precipitated was collected by filtration to give a total yield of 4.36 g (50%), as a cream solid. 1HNMR (300 MHz) (d6-DMSO, 100° C.)) δ 1.43 (9H, s), 1.75-2-20 (2H, 2×m), 2.75-3.1 (1H, br), 3.20-3.75 (4H, m), 4.09 (2H, s), 4.21 (2H, s), 6.22 (1H, br s), 6.37 2H, br t), 6.70 (1H, br), 6.99 (2H, d), 7.14 (2H, m) and 7.37 (2H, br t).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08071582B2 |
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| Source dataset | uspto-grants-2011_12 |
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| ORD ID | ord-8b49cd907e4b4880b5c9bc4225d54d74 |
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| Source note | uspto-grants-2011_12 |
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