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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2300963Generated: November 1, 2026

Sodium Methoxide → HCID 131723723, compound

https://huagongshe.com/reaction/2300963

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSodium MethoxideHCID 10942334—
ReactantHCID 88182850HCID 88182850—
SolventMethanolHCID 887—
ProductHCID 131723723HCID 131723723—

Reaction Conditions

Temperature0 °C

Reaction Steps

Thioacetic acid S-(trans-3-tert-butoxycarbonylamino-6-tert-butoxycarbonyloxy-4,4-diethyl-1,2,3,4-tetrahydro-naphthalen-2-yl) ester (234 mg, 0.47 mmol) in MeOH (5 mL) was added the sodium methoxide (54 μL, 0.95 mmol) and stirred at 0° C. for 30 min. The mixture was quenched with H2O, diluted with Et2O (50 mL), washed with H2O, HCl (10%), H2O, brine, dried over MgSO4. The residu was used without any other purification (151 mg, 71%). 1H NMR (CDCl3): 7.10-6.95 (3H, m, Har), 4.58 (1H, d, J=11.0 Hz, NH), 4.00 (1H, t, J=11 Hz, CHNH), 3.40-3.25 (2H, m), 2.98 (1H, m), 1.80-1.45 (22H, m), 0.80-0.70 (6H, m, CH3).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06498196B1
Source datasetuspto-grants-2002_12
ORD IDord-882fa6f08b23434abe081172b1f13f21
Source noteuspto-grants-2002_12