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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 623252Generated: October 29, 2026

Benzyl mercaptan → HCID 14305315, compound

https://huagongshe.com/reaction/623252

Reaction equation

Participants

RoleNameHCIDCharge
ReactantBenzyl mercaptanHCID 7509—
ReactantSodium hydrideHCID 24758—
ReactantHCID 14305314HCID 14305314—
SolventWaterHCID 962—
ProductHCID 14305315HCID 1430531527.2%

Reaction Steps

To a stirred suspension of 0.62 g (0.013 mol) of 50% sodium hydride (in mineral oil), which had been washed withh hexanes, in 20 mls dry dimethylformamide cooled to -5° under nitrogen was added dropwise 1.6 g (0.013 mol) benzyl mercaptan such that the temperature was maintained below 5°. The suspension was stirred at room temperature for 1 hour, cooled to 0°, and a solution of 2.0 g (0.012 mol) of the product from Example 1 was added dropwise while maintaining the temperature between 0° and 5°. After warming to room temperature, the solution was poured into water and extracted with ether. The combined organic layers were washed with water and with brine, dried over magnesium sulfate, and evaporatd to an oil which was purified by flash chromatography to afford 0.9 g (27%) oil: NMR (CDCl3, 200 MHz), 1.02 (3H, t J=7 Hz), 1.6 (2 H, m), 2.9 (2H, t, J=7 Hz), 4.45 (2H, s), 6.9-7.6 (7H, m), 8.3 (1H, m); IR (neat) 1560, 1370 cm-1.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04774337
Source datasetuspto-grants-1988_09
ORD IDord-abb4f57cff1c4cb887c7d331da7a29e9
Source noteuspto-grants-1988_09