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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 221581Generated: October 26, 2026

Benzyl Bromide → HCID 67156552, compound

https://huagongshe.com/reaction/221581

Reaction equation

Participants

RoleNameHCIDCharge
ReactantBenzyl BromideHCID 7498—
ReactantSodium CarbonateHCID 10340—
ReactantSodium hydrideHCID 24758—
ReactantMethyl trityl-L-threoninateHCID 11025190—
SolventDiethyl EtherHCID 3283—
SolventDimethylformamideHCID 6228—
ProductHCID 67156552HCID 6715655276.8%

Reaction Conditions

Temperature0 °C

Reaction Steps

A 250-mL, round-bottomed flask, under an atmosphere of N2, was charged with sodium hydride (60% oil dispersion, 772 mg, 19.3 mmol). The sodium hydride was washed with 3 portions of hexanes to remove the oil and then 8 mL of anhydrous DMF was added followed by benzyl bromide (3.38 mL, 28.4 mmol). The solution was cooled to 0° C. and then a solution of methyl N-trityl-L-threoninate (4.83 g, 12.9 mmol) dissolved in 12 mL of DMF was added dropwise via cannula over 5 minutes. After stirring for 2 hours, the reaction mixture was treated with saturated aqueous Na2CO3 solution and 200 mL of Et2O and the layers were separated. The organic portion was washed successively with H2O (5×100 mL) and brine (100 mL), dried over MgSO4, filtered and concentrated under reduced pressure. Chromatography (SiO2, 5-10% ethyl acetate/hexanes) gave 4.61 g of methyl O-benzyl-N-trityl-L-threoninate as a colorless syrup.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08207162B2
Source datasetuspto-grants-2012_06
ORD IDord-aba8e61ae4a348ddb0ff7d17846d3778
Source noteuspto-grants-2012_06