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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 475348Generated: October 26, 2026

Lithium hydroxide, monohydrate → (5R)-1-(chloroacetyl)-5-ethynyl-L-proline

https://huagongshe.com/reaction/475348

Reaction equation

Participants

RoleNameHCIDCharge
ReactantLithium hydroxide, monohydrateHCID 168937—
Reactantmethyl (5R)-1-(chloroacetyl)-5-((trimethylsilyl)ethynyl)-L-prolinateHCID 59683665—
SolventMethanolHCID 887—
SolventWaterHCID 962—
Product(5R)-1-(chloroacetyl)-5-ethynyl-L-prolineHCID 59683657—

Reaction Steps

To a stirred solution of methyl (5R)-1-(chloroacetyl)-5-((trimethylsilyl)ethynyl)-L-prolinate (3.69 g, 12.2 mmol) in MeOH (24 mL) and H2O (24 mL) at room temperature was added LiOH•H2O (0.8 g, 18 mmol). The reaction mixture was stirred at ambient temperature overnight and concentrated under reduced pressure. The residue was taken up in water and extracted with diethyl ether (2×). The aqueous layer was acidified to pH˜3 by adding 4% KHSO4 dropwise. The solution was extracted with ethyl acetate (3×). Combined ethyl acetate layers were washed with brine, dried (Na2SO4), filtered and concentrated under reduced pressure to provide the titled compound. MS (CI) m/z 216 (M+1)+.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08637546B2
Source datasetuspto-grants-2014_01
ORD IDord-a490cbbbb20943bd84ac2b815aa2a77c
Source noteuspto-grants-2014_01