Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2106490Generated: October 31, 2026

Tetrahydrofuran → HCID 57810547, compound

https://huagongshe.com/reaction/2106490

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTetrahydrofuranHCID 8028—
ReactantSodium borohydrideHCID 4311764—
ReactantHCID 68815437HCID 68815437—
ProductHCID 57810547HCID 5781054759%

Reaction Steps

A solution of (6-{1-[4-(3,3-Dimethyl-2-oxo-butoxy)-3-methyl-phenyl]-1-ethyl-propyl}-benzofuran-2-carbonyl)-amino]-acetic acid (66 mg, 0.130 mmol) (Example 57) in THF (2 mL) is treated with NaBH4 (11 mg, 0.26 mmol) at room temp. The resulting mixture is stirred for 2 hours. The mixture is concentrated and neutralized to pH 3 and extracted with EtOAc (3×5 mL). The organic layer is dried over sodium sulfate, concentrated to afford the desired compound (39 mg, 59%). MS (ES) m/e: 508.3 (M−1)

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07579488B2
Source datasetuspto-grants-2009_08
ORD IDord-f2a2d99223a34469946a5b40a2c9b685
Source noteuspto-grants-2009_08