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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

Reaction equation

Participants

RoleNameHCIDCharge
Reactant2-(Ethanesulfonyl)-1,3-benzothiazoleHCID 17428—
ReactantLithium HexamethyldisilazideHCID 2733832—
ReactantN-(tert-Butoxycarbonyl)-D-prolinalHCID 7009153—
SolventTetrahydrofuranHCID 8028—
ProductHCID 68710339HCID 68710339—

Reaction Conditions

Temperature0 °C

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

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07847100B2
Source datasetuspto-grants-2010_12
ORD IDord-4c3a89b674c54b2fa560a5376a4a68cb
Source noteuspto-grants-2010_12