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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1828055Generated: October 30, 2026

Benzyl Alcohol → HCID 58648572, compound

https://huagongshe.com/reaction/1828055

Reaction equation

Participants

RoleNameHCIDCharge
ReactantBenzyl AlcoholHCID 244—
ReactantDicyclohexylcarbodiimideHCID 10868—
ReactantBicyclo[2.2.1]heptane-1-methanesulfonic acid, 7,7-dimethyl-2-oxo-, (1S)-HCID 18462—
ReactantGpi-1485HCID 9837656—
Catalyst4-(Dimethylamino)pyridineHCID 14284—
SolventDichloromethaneHCID 6344—
ProductHCID 58648572HCID 5864857299.1%

Reaction Steps

A mixture of (2S)-1-(1,2-dioxo-3,3-dimethylpentyl)-2-pyrrolidine-carboxylic acid (500 mg; 2.07 mmol), benzyl alcohol (335 mg; 3.10 mmol), dicyclohexylcarbodiimide (683 mg; 3.31 mmol), 4-dimethylaminopyridine (84 mg; 0.69 mmol) and camphorsulphonic acid (160 mg; 0.69 mmol) in methylene chloride (30 mL) was stirred overnight under a nitrogen atmosphere. The reaction mixture was filtered through Celite to remove solids and concentrated in vacuo, and the crude material was purified on a flash column (25% ethyl acetate in hexane) to obtain 680 mg of the product as a colorless oil. 1H NMR (CDCl3; 300 MHz) δ 0.85 (t, 3H); 1.19 (s, 3H); 1.22 (s, 3H); 1.61–2.25 (m, 6H); 3.46–3.56 (m, 2H); 4.58 (dm, 1H); 5.18 (d, 2H, 7.35 (br, 5H).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07056935B2
Source datasetuspto-grants-2006_06
ORD IDord-c0eb2e5503864e6ab2fc913be4c90800
Source noteuspto-grants-2006_06