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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1824416Generated: November 1, 2026

Thionyl Chloride → 5-Allyloxy-pyrrolidine-2-carboxylic acid methyl ester hydrochloride

https://huagongshe.com/reaction/1824416

Reaction equation

Participants

RoleNameHCIDCharge
ReactantThionyl ChlorideHCID 24386—
Reactant5-Allyloxy-pyrrolidine-1,2-dicarboxylic acid 1-tert-butyl ester 2-methyl esterHCID 69584601—
SolventMethanolHCID 887—
Product5-Allyloxy-pyrrolidine-2-carboxylic acid methyl ester hydrochlorideHCID 6958449695%

Reaction Steps

To a solution of 5-allyloxy-pyrrolidine-1,2-dicarboxylic acid 1-tert-butyl ester 2-methyl ester, 4, (7.28 g, 27 mmol) in MeOH is added thionyl chloride (4 mL, 54 mmol). The solution is stirred overnight and the solvent removed in vacuo to afford 4.25 g (95% yield) of the desired product as a dark yellow crystal. 1H-NMR (300 MHz, CDCl3): δ 11.47 (s, 1H), 8.15 (s, 1H), 5.81 (m, 1H), 5.23 (m, 2H), 4.55 (s, 1H), 3.85 (s, 3H), 2.88 (m, 1H), 2.59–2.42 (m, 2H), 2.24 (m, 1H), 1.81 (m, 1H). 13C-NMR (75.5 MHz, CDCl3): δ 170.0, 132.7, 132.3, 120.2, 119.6, 60.6, 60.2, 59.4, 58.9, 53.9, 36.6, 29.5, 29.2, 28.3. ESI MS 170.13 (M+H).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07041696B2
Source datasetuspto-grants-2006_05
ORD IDord-25146b4edb73476b8979191abba6eeb8
Source noteuspto-grants-2006_05