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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1438154Generated: November 1, 2026

o-Fluorobenzaldehyde → 2-(Ethylsulfanyl)benzaldehyde

https://huagongshe.com/reaction/1438154

Reaction equation

Participants

RoleNameHCIDCharge
Reactanto-FluorobenzaldehydeHCID 67970—
Reactant2-(Isopropylthio)benzaldehydeHCID 11206137—
Product2-(Ethylsulfanyl)benzaldehydeHCID 1308272678%

Reaction Steps

114A (10.4 g, 78% yield) was prepared from 2-fluorobezaldehyde (10 g, 81 mmol) and thioethane (5.5 g, 89 mmol) using a procedure similar to that used in the preparation of 11A. 1H NMR (400 MHz, Methanol-d4) δ ppm 1.23-1.42 (m, 3H) 2.98 (q, J=7.34 Hz, 2H) 7.17-7.37 (m, 1H) 7.38-7.64 (m, 2H) 7.81 (dd, J=7.70, 1.59 Hz, 1H) 10.30 (s, 1H).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07622585B2
Source datasetuspto-grants-2009_11
ORD IDord-2e00be5c901147ababb9c93327081b03
Source noteuspto-grants-2009_11