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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2168181Generated: October 31, 2026

Hydrochloric Acid → HCID 58208637, compound

https://huagongshe.com/reaction/2168181

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydrochloric AcidHCID 313—
ReactantHydrogen PeroxideHCID 784—
ReactantSodium SulfiteHCID 24437—
ReactantLithium hydroxide, monohydrateHCID 168937—
ReactantSodium BicarbonateHCID 516892—
ReactantHCID 58208607HCID 58208607—
SolventWaterHCID 962—
SolventTetrahydrofuranHCID 8028—
ProductHCID 58208637HCID 5820863776%

Reaction Conditions

Temperature0 °C

Reaction Steps

Aqueous hydrogen peroxide solution (30% 1.15 mL) was added to a stirred solution of Boc-protected intermediate (135) (1.02 g, 2.45 mmol) in a mixture of tetrahydrofuran (30 mL) and water (9 mL) at 0° C. Lithium hydroxide monohydrate (128 mg, 3.04 mmol) was added then the mixture was stirred at 0° C. for 1 h, then overnight at ambient temperature. A further aliquot of hydrogen peroxide solution (30% 0.575 mL) was added followed by lithium hydroxide monohydrate (64 mg and stirring continued at ambient temperature for 3 h. A solution of sodium sulphite (1.87 g) in water (10 mL) was then added followed by aqueous sodium hydrogen carbonate solution (30 mL). The mixture was stirred for 5 minutes then the volume reduced by half in vacuo (≧25 mbar, external water bath 25° C.). Water (50 mL) was added then the pH adjusted to ≦2 using 5M hydrochloric acid. The aqueous phase was, extracted with dichloromethane (4×50 mL), then the combined organic layers were dried (Na2SO4), filtered and reduced in vacuo to leave a pale yellow oil. The oil was partitioned between a solution of sodium carbonate (1.4 g) in water (50 mL) and diethyl ether (20 mL). The aqueous layer was re-extracted with diethyl ether (3×20 mL) then the pH adjusted to ≦2 using 5M hydrochloric acid. The acidified aqueous layer was then extracted with diethyl ether (3×20 mL) then the combined organic layers dried (MgSO4), filtered and reduced in vacuo to leave acid (136) as a colourless gum (Yield 475 mg, 76%). Analytical HPLC, Rt=16.74 min., HPLC-MS 156.1 [M−Boc+2H]+, 220.1 [M+2H−tBu]+, 537.3 [2M+Na]+; [α]D21+27.2° (c=2.576, CHCl3). δH (500 MHz, CDCl3) 0.90 (3H, s, CH3C), 1.35-1.45+1.61-1.81 (8H, m, 4×CH2), 1.45 (9H, s, (CH3)3C), 4.18 (1H, d, J=9.2, NCB), 5.12 (1H, d, J=8.95, NH), 8.7-10.0 (1H, b, COOH); δC (125 MHz, CDCl3) 22.26/22.41/22.66 (CH3C), 23.85/24.08/24.32/24.61/25.91+36.88/36.94 (4×CH2), 28.30 ((CH3)3C), 45.03/45.61 (CH3C), 60.84 (NHCH), 79.98 ((CH3)3C), 155.76/156.46 (NHC═O), 177.04 (CHC═O).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09045492B2
Source datasetuspto-grants-2015_06
ORD IDord-7767cc226e17404790b6570661785b18
Source noteuspto-grants-2015_06