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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1993123Generated: November 4, 2026

Sulfuric Acid → HCID 68612479, compound

https://huagongshe.com/reaction/1993123

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSulfuric AcidHCID 1118—
ReactantN-[(Phenylmethoxy)carbonyl]-L-tyrosine methyl esterHCID 7010613—
SolventDichloromethaneHCID 6344—
ProductHCID 68612479HCID 6861247962%

Reaction Conditions

Temperature0 °C

Reaction Steps

H-D-Tyr-O-me hydrochloride 2.1 (25 g, 107.7 mmol) is dissolved in methylene chloride (150 mL) and aqueous sodium bicarbonate (22 g in 150 mL water), and then cooled to 0° C. To this resulting solution benzyl chloroformate (20 g, 118 mmol) is slowly added. After complete addition, the resulting solution is warmed to room temperature, and is then stirred for 2 h. The organic phase is separated, dried over Na2SO4, and concentrated under reduced pressure, to give the crude carbamate 2.2 (35 g). The crude CBZ-Tyr-OMe product is dissolved in methylene chloride (300 mL) containing concentrated H2SO4. Isobutene is bubbled though the solution for 6 h. The reaction is then cooled to 0° C., and neutralized with saturated NaHCO3 aqueous solution. The organic phase is separated, dried, concentrated under reduced pressure, and purified by silica gel column chromatography to afford the tert-butyl ether 2.3 (25.7 g, 62%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07649015B2
Source datasetuspto-grants-2010_01
ORD IDord-13fe3210d6a74112b109acd79734f875
Source noteuspto-grants-2010_01