HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2261901Generated: November 3, 2026
2-(Ethanesulfonyl)-1,3-benzothiazole → HCID 68710339, compound
https://huagongshe.com/reaction/2261901
Participants
| Role | Name | HCID | Charge |
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| Reactant | 2-(Ethanesulfonyl)-1,3-benzothiazole | HCID 17428 | — |
| Reactant | Lithium Hexamethyldisilazide | HCID 2733832 | — |
| Reactant | N-(tert-Butoxycarbonyl)-D-prolinal | HCID 7009153 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | HCID 68710339 | HCID 68710339 | — |
Reaction Steps
To a stirring solution of Boc-D-Prolinal (0.53 g, 2.65 mmol) and 2-(ethyl sulfonyl)-1,3-benzothiazole (1.5 g, 6.62 mmol) in tetrahydrofuran (4 mL) at −78° C. was added 1M Lithium bis(trimethylsilyl)amide in THF (4 mL) and continued stirring for 30 min. Then the mixture was warmed to 0° C. and stirred for an additional 3 hr. Upon completion via LC-MS, the reaction mixture was quenched with 20% ammonium chloride solution and extracted with ethyl ether. The ether layer washed with brine, dried over sodium sulfate anhydrous, filtered and dried in vacuo to yield crude product which was further purified on an ISCO normal phase HPLC using a 100% to 75% gradient of hexane to ethyl acetate as mobile phase. Pure tert-butyl-(2R)-2-[(1E)-prop-1-enyl]pyrrolidine-1-carboxylate was isolated from the combined fractions (0.09 g). 1H NMR (CD3OD, 400 Mhz) 5.51-5.44 ppm (m, 1H), 5.39-5.31 (m, 1H), 4.20-4.12 (m, 1H), 3.38-3.30 (m, 3H), 1.91-1.81 (m, 2H), 1.79-1.66 (m, 4H), 1.425 (s, 9H).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07847100B2 |
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| Source dataset | uspto-grants-2010_12 |
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| ORD ID | ord-4c3a89b674c54b2fa560a5376a4a68cb |
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| Source note | uspto-grants-2010_12 |
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