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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1706161Generated: October 25, 2026

Hydrochloric Acid → 1-benzoyl-5-chloromethyl-2,3-dihydro-1H-indole

https://huagongshe.com/reaction/1706161

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydrochloric AcidHCID 313—
ReactantFormaldehydeHCID 712—
Reactant1-benzoyl-2,3-dihydro-1H-indoleHCID 681214—
ReactantCarbon tetrachloride hexaneHCID 21584008—
SolventAcetic AcidHCID 176—
Product1-benzoyl-5-chloromethyl-2,3-dihydro-1H-indoleHCID 1302142860%

Reaction Steps

1-Benzoyl-2,3-dihydro-1H-indole (Beilstein, 20, 257) (5.58 g, 25 mmole) is dissolved in 50 ml of glacial acetic acid, then 56 ml (ca 70 mmoles) of 40% formaldehyde are added, and dry hydrogen chloride passed into the solution which is maintained at 70° for 3 hours. The solution is evaporated, and the residue dissolved in benzene, and again evaporated to dryness to give 6.53 g of crude product. This residue is treated with carbon tetrachloride-hexane to give 4.05 g (60%) of 1-benzoyl-5-chloromethyl-2,3-dihydro-1H-indole, m.p. 107.5°-110.0°.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04206216
Source datasetuspto-grants-1980_06
ORD IDord-f2e3112c0a7e44cda6ac5fdab2c018f7
Source noteuspto-grants-1980_06