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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1948658Generated: October 31, 2026

Benzoyl chloride → HCID 59450538, compound

https://huagongshe.com/reaction/1948658

Reaction equation

Participants

RoleNameHCIDCharge
ReactantBenzoyl chlorideHCID 7412—
ReactantTriethylamineHCID 8471—
Reactant5-Hydroxy-1-indanoneHCID 233147—
Catalyst4-(Dimethylamino)pyridineHCID 14284—
SolventDichloromethaneHCID 6344—
ProductHCID 59450538HCID 59450538—

Reaction Steps

Benzoyl chloride (126.9 g, 0.900 mol) was added slowly to a stirred mixture of the product of Step A (121 g, 0.818 mol), triethylamine (99.1 g, 0.982 mol) and catalytic amount of DMAP (1 g, 8.18 mmol) in dichloromethane (1 L) at rt under nitrogen. The mixture was stirred overnight and diluted with dichloromethane (1 L). Then the solution was washed with water, hydrochloric acid (0.5 M, 2×1 L), and brine. The organic layer was dried over MgSO4, filtered and the solvent was evaporated under reduced pressure. The residue was dried in vacuo to give the compound. 1H-NMR (400 MHz, CDCl3): δ 8.19-8.22 (m, 2H), 7.83 (d, J=8.1 Hz, 1H), 7.65-7.69 (m, 1H), 7.52-7.55 (m, 2H), 7.37 (s, 1H), 7.22 (dd, J=8.1 Hz, J=2.0 Hz, 1H), 3.17-3.20 (m, 2H), 2.73-2.76 (m, 2H) ppm.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08399507B2
Source datasetuspto-grants-2013_03
ORD IDord-1c6d8439d57544c280c7c2910485c98e
Source noteuspto-grants-2013_03