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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1585142Generated: November 1, 2026

Methyl iodide → HCID 15431767, compound

https://huagongshe.com/reaction/1585142

Reaction equation

Participants

RoleNameHCIDCharge
ReactantMethyl iodideHCID 6328—
ReactantCarbon DisulfideHCID 6348—
ReactantAmmonium HydroxideHCID 14923—
ReactantSodium hydrideHCID 24758—
ReactantN-Boc-D-phenylalaninolHCID 7019371—
ProductHCID 15431767HCID 1543176791%

Reaction Conditions

Temperature0 °C

Reaction Steps

In a 500 mL flask equipped with magnetic stirrer, N-(t-butyloxycarbonyl)-(D)-phenylalaninol(0.040 mole, 10.05 g) was dissolved in 200 mL of THf and was added with NaH(0.048 mole, 1.15 g) at 0° C. The reaction mixture was stirred at 0° C. for 1 hour, followed by the addition of CS2 (0.048 mole, 3.65 g). After being stirred for 40 min. at 0° C., MeI(0.048 mole, 6.81 g) was added to the reaction mixture. The reaction mixture was stirred at room temperature for 2 hours, followed by the addition of 5N NH4OH (0.090 mole, 18.0 mL) for 6 hours. The resulting solution was quenched with water. The organic layer was extracted 3 times with dichloromethane, dried over magnesium sulfate and distilled in vacuo, to give a solid. This was recrystalized in a solution mixture of n-hexane and diethyl ether, to produce 11.3 g of O-thiocarbamoyl-N-(t-butyloxycarbonyl)-(D)-phenylalaninol: Yield 78%.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05935997
Source datasetuspto-grants-1999_08
ORD IDord-a03109875335451089757cc5054e5449
Source noteuspto-grants-1999_08