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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1686869Generated: November 2, 2026

HCID 59189493, compound → HCID 86639081, compound

https://huagongshe.com/reaction/1686869

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHCID 59189493HCID 59189493—
Reactant(1s)-Camphanoyl chlorideHCID 71432218—
Catalyst4-(Dimethylamino)pyridineHCID 14284—
SolventDichloromethaneHCID 6344—
ProductHCID 86639081HCID 8663908191%

Reaction Steps

Under a nitrogen atmosphere, (1S)-camphanic acid chloride (1.68 g, 7.77 mmol) was added to a solution of (RS)-1-(4-iodo-2-nitrophenyl)-2,2-dimethyl-1-propanol (2.17 g, 6.47 mmol) and DMAP (1.18 g, 9.7 mmol) in anhydrous dichloromethane (50 mL). The mixture was stirred overnight at room temperature and then washed with saturated NaHCO3 solution (60 mL) and water (60 mL). The organic phase was dried over Na2SO4, concentrated in vacuo and purified by silica gel column chromatography to yield (RS)-1-(4-iodo-2-nitrophenyl)-2,2-dimethyl-1-propyl (1S)-camphanate (2.94 g, 88%, 1:1 mixture of diastereomers) as a white solid. 1H NMR (400 MHz, CDCl3) for diastereomers: δ 8.23 (m, 1H, Ph-H), 7.90 (m, 1H, Ph-H), 7.31 (m, 1H, Ph-H), 6.56 and 6.51 (2 s, 1H, Ph-CH), 2.38 (m, 1H), 2.07-1.9 (m, 2H), 1.69 (m, 1H), 1.13, 1.11, 1.07, 1.04, 1.02, 0.87 (6 s, 9H, CH3×3), 0.96 (s, 9H, (CH3)3C).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08148503B2
Source datasetuspto-grants-2012_04
ORD IDord-b507b7637dce433e93133dc7e87473d2
Source noteuspto-grants-2012_04