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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 854007Generated: October 29, 2026

Hexane → HCID 69221993, compound

https://huagongshe.com/reaction/854007

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHexaneHCID 8058—
ReactantSodium hydrideHCID 24758—
ReactantPropyltriphenylphosphonium bromideHCID 80374—
Reactant1-(tert-Butoxycarbonyl)-4-oxopiperidine-2-carboxylic acidHCID 46835694—
SolventWaterHCID 962—
SolventTetrahydrofuranHCID 8028—
ProductHCID 69221993HCID 69221993—

Reaction Steps

Propyltriphenylphosphonium bromide (1.24 g, 3.22 mmol) in THF (10 mL) was added to hexane washed sodium hydride (123 mg, 3.22 mmol), in THF (10 mL) and stirred at room temperature for 3 h. Methyl ester 12a (P=Boc, m=2, P2=Me) (0.55 g, 2.15 mmol) in THF (5 mL) was added to the above reaction mixture slowly and then allowed to stir for additional 2 h. It was then poured into water and extracted with ethyl acetate (30 mL). The organic phase was dried with magnesium sulfate, filtered and evaporated to dryness, the resulting residue was chromatographed using 20% EtOAc in hexanes to provide the product 4-propylidene-piperidine-1,2-dicarboxylic acid 1-tert-butyl ester 2-methyl ester. (0.100 g, 16%): MS (ESPOS): 284 [M+H]+; 1H NMR (300 MHz, CD3OD) δ 5.18 (m, m), 4.60-4.93 (m, 1), 3.91 (m, 1), 3.67 (s, 3), 2.94-3.04 (m, 2), 2.40-2.48 (m, 2), 1.99-2.06 (m, 1), 1.85-1.97 (m, 2), 1.38 (bs, 9), 0.85 (t, J=5 Hz, 3).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07256177B2
Source datasetuspto-grants-2007_08
ORD IDord-09ebda8176aa4c6da53f2a3b8f3f4117
Source noteuspto-grants-2007_08