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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1367728Generated: October 31, 2026

Sodium Hydroxide → HCID 66770098, compound

https://huagongshe.com/reaction/1367728

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSodium HydroxideHCID 14798—
ReactantHCID 66769938HCID 66769938—
SolventTetrahydrofuranHCID 8028—
ProductHCID 66770098HCID 6677009869%

Reaction Steps

A solution of [(1-benzyloxycarbonylamino-2-vinyl-cyclopropyl)-ethoxy-phosphinoyl]-acetic acid ethyl ester (352 mg, 0.89 mmol) in THF (3 mL) was stirred at 0° C. as 1 N NaOH (980 μL, 0.98 mmol) was added. The solution was stirred overnight at r.t. and then concentrated, diluted with H2O (10 mL) and washed with ethyl acetate. The aqueous layer was acidified with 1 N HCl (5 mL) and extracted with ethyl acetate (×2). The organic extracts were washed with H2O, dried (MgSO4) and concentrated to yield [(1-Benzyloxycarbonylamino-2-vinyl-cyclopropyl)-ethoxy-phosphinoyl]-acetic acid (224 mg, 69%). 1H NMR (300 MHz, CDCl3): δ 7.34 (s, 5H), 5.91 (m, 2H), 5.20 (m, 2H), 4.21 (m, 2H), 3.11 (m, 2H), 2.30 (m, 1H), 2.03 (m, 1H), 1.85 (m, 2H), 1.70 (m, 2H), 1.58 (m, 2H), 1.38 (m, 2H), 1.25 (m, 3H). 31P (121.4 MHz, CDCl3): 45.109, 41.119, 40.965, 39.514

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07893264B2
Source datasetuspto-grants-2011_02
ORD IDord-bbc52a9a35de4f6a84f6d7d8ea818405
Source noteuspto-grants-2011_02