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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2252385Generated: October 30, 2026

Benzyl Bromide → HCID 69300327, compound

https://huagongshe.com/reaction/2252385

Reaction equation

Participants

RoleNameHCIDCharge
ReactantBenzyl BromideHCID 7498—
ReactantSodium BicarbonateHCID 516892—
ReactantLithium diisopropylamide mono(tetrahydrofuran)HCID 10997623—
ReactantHCID 69299180HCID 69299180—
SolventTetrahydrofuranHCID 8028—
ProductHCID 69300327HCID 69300327—

Reaction Steps

In 5 mL of THF, 145 mg (0.35 mmol) of 1-(3-benzyloxy-17-cyclopropylmethyl-4,5α-epoxy-14-hydroxy-morphinan-6β-yl)-pyrrolidin-2-one obtained in Example 47-1 was dissolved, and 2.84 mL (1.02 mmol) of 0.36 N LDA/THF solution was added at −78° C., followed by stirring the mixture for 1 hour. Thereafter, 0.10 mL (0.87 mmol) of benzyl bromide was added thereto and the resulting mixture was stirred for 3 hours. To this reaction solution, aqueous saturated sodium hydrogen carbonate solution was added and the resulting mixture was extracted with chloroform. Organic layers were combined, washed with saturated saline, dried over anhydrous magnesium sulfate and concentrated to obtain 1-(3-benzyloxy-17-cyclopropylmethyl-4,5α-epoxy-14-hydroxy-morphinan-6β-yl)-3-benzyl-pyrrolidin-2-one as a crude product.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07320984B2
Source datasetuspto-grants-2008_01
ORD IDord-97e3e32cc1944cdaa032015503c0002b
Source noteuspto-grants-2008_01