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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1582072Generated: November 1, 2026

Oxalyl chloride → HCID 22719746, compound

https://huagongshe.com/reaction/1582072

Reaction equation

Participants

RoleNameHCIDCharge
ReactantOxalyl chlorideHCID 65578—
ReactantHCID 22719744HCID 22719744—
SolventDichloromethaneHCID 6344—
ProductHCID 22719746HCID 22719746—

Reaction Steps

Oxalyl chloride (1.15 ml, 13.2 mmol) was added to an ice-cooled solution of 1-{2-[(benzyloxy)carbonyl]pentyl}cyclopentanecarboxylic acid (EP 274234) (2.0 g, 6.3 mmol) in dry dichloromethane (20 ml), and the solution stirred at room temperature for 2 hours. The reaction mixture was concentrated under reduced pressure and the residue azetroed with dichloromethane (3×), to give the title compound as a golden oil, 2.1 g; 1H NMR (CDCl3, 300 MHz) δ: 0.88 (t, 3H), 1.28 (m, 2H), 1.43 (m, 2H), 1.63 (m, 6H), 2.00 (m, 1H), 2.08-2.35 (m, 3H), 2.44 (m, 1H), 5.15 (s, 2H), 7.28 (m, 5H).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06734186B1
Source datasetuspto-grants-2004_05
ORD IDord-13f6d18069d94c9d88fa1b959ef60687
Source noteuspto-grants-2004_05