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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2246061Generated: November 3, 2026

Benzene, (3-bromopropoxy)- → HCID 86616554, compound

https://huagongshe.com/reaction/2246061

Reaction equation

Participants

RoleNameHCIDCharge
ReactantBenzene, (3-bromopropoxy)-HCID 68522—
ReactantSodium ethanethiolateHCID 4459711—
SolventEthanolHCID 702—
ProductHCID 86616554HCID 86616554—

Reaction Steps

Sodium ethanethiolate (6 mmol, 0.5 g) and 3-phenoxypropyl bromide (5 mmol, 1.1 g) in ethanol were refluxed overnight. After removal of solvent, Ether was added, washed with H20 and evaporated to give 3-phenoxypropylethyl sulfide. It was treated with 1 equivalent of acrylic acid in acetone in the presence of 4 equivalents of 12 N HCl under N2 at room temperature overnight and then at 50° C. for 3 h, affording 3-(S-ethyl-3-phenoxypropylsulfoniumyl)propionic acid chloride as a white powder. It was then subjected to the general procedure 1 to give compound 573 as a white powder (0.58 g, 25% overall yield). Anal. (C14H22Na2O8P2S.0.5 H2O) C, H.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07687482B2
Source datasetuspto-grants-2010_03
ORD IDord-8853705a31b347c3addb2af59deabdb2
Source noteuspto-grants-2010_03